The Molecular Genetics of Keratin Disorders (Q34189864)

31 July 2017

1 reference

title

The molecular genetics of keratin disorders (English)

1 reference

31 July 2017

The Molecular Genetics of Keratin Disorders (English)

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

23 December 2023

1 reference

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

23 December 2023

author name string

Frances Smith

1

1 reference

31 July 2017

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=12688839

23 December 2023

publication date

1 January 2003

1 reference

American Journal of Clinical Dermatology

31 July 2017

published in

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31 July 2017

volume

4

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31 July 2017

issue

5

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31 July 2017

page(s)

347-364

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Chromosomal assignments of human type I and type II cytokeratin genes to different chromosomes.

31 July 2017

cites work

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1 reference

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A group of type I keratin genes on human chromosome 17: characterization and expression

23 December 2023

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Three epidermal and one simple epithelial type II keratin genes map to human chromosome 12

23 December 2023

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Sequence comparisons of intermediate filament chains: evidence of a unique functional/structural role for coiled-coil segment 1A and linker L1

23 December 2023

6

1 reference

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Concurrence between the molecular overlap regions in keratin intermediate filaments and the locations of keratin mutations in genodermatoses

23 December 2023

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1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Structure, Function, and Dynamics of Keratin Intermediate Filaments

23 December 2023

8

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Epidermal keratin filaments assembled in vitro have masses-per-unit-length that scale according to average subunit mass: structural basis for homologous packing of subunits in intermediate filaments

23 December 2023

9

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

The intermediate filament protein consensus motif of helix 2B: its atomic structure and contribution to assembly

23 December 2023

10

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The catalog of human cytokeratins: patterns of expression in normal epithelia, tumors and cultured cells

23 December 2023

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Epidermolysis bullosa in Northern Ireland

23 December 2023

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Epidermolysis bullosa. Application of epidemiologic principles to the study of a group of rare diseases via a disease registry.

23 December 2023

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The prevalence of epidermolysis bullosa in Scotland

23 December 2023

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Epidermolysis bullosa resembling juvenile dermatitis herpetiformis

23 December 2023

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Revised clinical and laboratory criteria for subtypes of inherited epidermolysis bullosa. A consensus report by the Subcommittee on Diagnosis and Classification of the National Epidermolysis Bullosa Registry

23 December 2023

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https://api.crossref.org/works/10.2165/00128071-200304050-00005

Epidermolysis Bullosa Simplex (Dowling-Meara Type) Is a Genetic Disease Characterized by an Abnormal Keratin-Filament Network Involving Keratins K5 and K14

23 December 2023

18

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Epidermolysis bullosa simplex (Dowling-Meara). A clinicopathological review

23 December 2023

19

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https://api.crossref.org/works/10.2165/00128071-200304050-00005

A function for keratins and a common thread among different types of epidermolysis bullosa simplex diseases

23 December 2023

24

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Mutant keratin expression in transgenic mice causes marked abnormalities resembling a human genetic skin disease

23 December 2023

25

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities

23 December 2023

26

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: Genetic and functional analyses

23 December 2023

27

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A mutation in the conserved helix termination peptide of keratin 5 in hereditary skin blistering

23 December 2023

28

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

The expression of mutant epidermal keratin cDNAs transfected in simple epithelial and squamous cell carcinoma lines

23 December 2023

29

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Expression of mutant keratin cDNAs in epithelial cells reveals possible mechanisms for initiation and assembly of intermediate filaments

23 December 2023

30

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Linkage of epidermolysis bullosa simplex to keratin gene loci

23 December 2023

34

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Human keratin diseases: hereditary fragility of specific epithelial tissues

23 December 2023

35

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Exempting Homologous Pseudogene Sequences from Polymerase Chain Reaction Amplification Allows Genomic Keratin 14 Hotspot Mutation Analysis

23 December 2023

36

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

DNA based prenatal testing for the skin blistering disorder epidermolysis bullosa simplex

23 December 2023

37

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A premature stop codon mutation in the 2B helix termination peptide of keratin 5 in a German epidermolysis bullosa simplex Dowling-Meara case

23 December 2023

38

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Donor splice site mutation in keratin 5 causes in-frame removal of 22 amino acids of H1 and 1A rod domains in Dowling-Meara epidermolysis bullosa simplex

23 December 2023

39

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Expression of a truncated keratin 5 may contribute to severe palmar--plantar hyperkeratosis in epidermolysis bullosa simplex patients

23 December 2023

40

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A common keratin 5 gene mutation in epidermolysis bullosa simplex--Weber-Cockayne

23 December 2023

41

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A novel three-nucleotide deletion in the helix 2B region of keratin 14 in epidermolysis bullosa simplex: delta E375.

23 December 2023

42

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Severe palmo-plantar hyperkeratosis in Dowling-Meara epidermolysis bullosa simplex caused by a mutation in the keratin 14 gene (KRT14)

23 December 2023

43

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Keratin 14 point mutations at codon 119 of helix 1A resulting in different epidermolysis bullosa simplex phenotypes

23 December 2023

44

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Keratin 14 gene mutations in patients with epidermolysis bullosa simplex

23 December 2023

45

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Partial Dominance of a Keratin 14 Mutation in Epidermolysis Bullosa Simplex — Increased Severity of Disease in a Homozygote

23 December 2023

46

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

The genetic basis of epidermolysis bullosa simplex with mottled pigmentation

23 December 2023

49

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation

23 December 2023

50

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A missense mutation in the rod domain of keratin 14 associated with recessive epidermolysis bullosa simplex.

23 December 2023

51

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A human keratin 14 "knockout": the absence of K14 leads to severe epidermolysis bullosa simplex and a function for an intermediate filament protein

23 December 2023

52

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplex

23 December 2023

53

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A functional "knockout" of human keratin 14

23 December 2023

54

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Effects of keratin 14 ablation on the clinical and cellular phenotype in a kindred with recessive epidermolysis bullosa simplex

23 December 2023

55

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A keratin 14 'knockout' mutation in recessive epidermolysis bullosa simplex resulting in less severe disease

23 December 2023

56

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

The basal keratin network of stratified squamous epithelia: defining K15 function in the absence of K14.

23 December 2023

57

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Complete cytolysis and neonatal lethality in keratin 5 knockout mice reveal its fundamental role in skin integrity and in epidermolysis bullosa simplex

23 December 2023

58

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Selective involvement of keratins K1 and K10 in the cytoskeletal abnormality of epidermolytic hyperkeratosis (bullous congenital ichthyosiform erythroderma)

23 December 2023

59

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Transgenic mice expressing a mutant keratin 10 gene reveal the likely genetic basis for epidermolytic hyperkeratosis

23 December 2023

60

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Linkage of the epidermolytic hyperkeratosis phenotype and the region of the type II keratin gene cluster on chromosome 12.

23 December 2023

61

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q

23 December 2023

62

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

The genetic basis of epidermolytic hyperkeratosis: a disorder of differentiation-specific epidermal keratin genes.

23 December 2023

63

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A leucine----proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis

23 December 2023

64

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Mutations in the rod domains of keratins 1 and 10 in epidermolytic hyperkeratosis

23 December 2023

65

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

An Atypical Form of Bullous Congenital Ichthyosiform Erythroderma is Caused by a Mutation in the L12 Linker Region of Keratin 1

23 December 2023

66

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Epidermolytic hyperkeratosis: applied molecular genetics

23 December 2023

67

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Arginine in the beginning of the 1A rod domain of the keratin 10 gene is the hot spot for the mutation in epidermolytic hyperkeratosis

23 December 2023

68

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Cytokeratin No. 9, an epidermal type I keratin characteristic of a special program of keratinocyte differentiation displaying body site specificity.

23 December 2023

69

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Distribution of a special subset of keratinocytes characterized by the expression of cytokeratin 9 in adult and fetal human epidermis of various body sites

23 December 2023

70

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Genetic and Clinical Mosaicism in a Type of Epidermal Nevus

23 December 2023

71

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Birthmark due to cutaneous mosaicism for keratin 10 mutation

23 December 2023

72

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Phenotypic heterogeneity in bullous congenital ichthyosiform erythroderma: possible somatic mosaicism for keratin gene mutation in the mildly affected mother of the proband

23 December 2023

73

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A novel dinucleotide mutation in keratin 10 in the annular epidermolytic ichthyosis variant of bullous congenital ichthyosiform erythroderma

23 December 2023

74

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A novel helix termination mutation in keratin 10 in annular epidermolytic ichthyosis, a variant of bullous congenital ichthyosiform erythroderma

23 December 2023

75

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Cyclic ichthyosis with epidermolytic hyperkeratosis: A phenotype conferred by mutations in the 2B domain of keratin K1

23 December 2023

76

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Epidermolytic hyperkeratosis with polycyclic psoriasiform plaques resulting from a mutation in the keratin 1 gene

23 December 2023

77

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Ichthyosis bullosa of Siemens--a disease involving keratin 2e

23 December 2023

79

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Characterization of human cytokeratin 2, an epidermal cytoskeletal protein synthesized late during differentiation

23 December 2023

80

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Genetic linkage of the keratin type II gene cluster with ichthyosis bullosa of Siemens and with autosomal dominant ichthyosis exfoliativa

23 December 2023

81

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Ichthyosis bullosa of Siemens is caused by mutations in the keratin 2e gene

23 December 2023

82

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Mutations in the rod domain of keratin 2e in patients with ichthyosis bullosa of Siemens

23 December 2023

83

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Pachyonychia congenita; a report of six cases in one family, with a note on linkage data

23 December 2023

84

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Keratin 16 and keratin 17 mutations cause pachyonychia congenita

23 December 2023

85

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Novel proline substitution mutations in keratin 16 in two cases of pachyonychia congenita type 1

23 December 2023

86

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Mutation of a type II keratin gene (K6a) in pachyonychia congenita

23 December 2023

87

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Identification of sporadic mutations in the helix initiation motif of keratin 6 in two pachyonychia congenita patients: further evidence for a mutational hot spot

23 December 2023

88

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita.

23 December 2023

89

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Delayed-onset pachyonychia congenita associated with a novel mutation in the central 2B domain of keratin 16.

23 December 2023

90

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A mutation in the V1 domain of K16 is responsible for unilateral palmoplantar verrucous nevus

23 December 2023

91

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21

23 December 2023

92

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Keratin 17 expression in the hard epithelial context of the hair and nail, and its relevance for the pachyonychia congenita phenotype

23 December 2023

94

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Novel keratin 17 mutations in pachyonychia congenita type 2.

23 December 2023

95

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2

23 December 2023

96

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2.

23 December 2023

97

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex

23 December 2023

98

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

The inherited palmoplantar keratodermas

23 December 2023

99

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Ultrastructural changes resulting from keratin-9 gene mutations in two families with epidermolytic palmoplantar keratoderma

23 December 2023

101

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Mapping of a gene for epidermolytic palmoplantar keratoderma to the region of the acidic keratin gene cluster at 17q12-q21.

23 December 2023

102

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK).

23 December 2023

103

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Epidermolytic palmoplantar keratoderma due to a novel type of keratin mutation, a 3-bp insertion in the keratin 9 helix termination motif

23 December 2023

104

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Novel splice site mutation in keratin 1 underlies mild epidermolytic palmoplantar keratoderma in three kindreds

23 December 2023

105

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A mutation in the V1 end domain of keratin 1 in non-epidermolytic palmar-plantar keratoderma

23 December 2023

106

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Evidence for novel functions of the keratin tail emerging from a mutation causing ichthyosis hystrix

23 December 2023

107

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Evidence against keratin gene mutations in a family with ichthyosis hystrix Curth-Macklin

23 December 2023

108

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Novel mutations in keratin 16 gene underly focal non-epidermolytic palmoplantar keratoderma (NEPPK) in two families

23 December 2023

109

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Novel keratin 16 mutations and protein expression studies in pachyonychia congenita type 1 and focal palmoplantar keratoderma

23 December 2023

110

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

23 December 2023

White sponge nevus

111

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Ultrastructure of the white sponge nevus

23 December 2023

112

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

White sponge nevus (leukoedema exfoliativum mucosae oris): Ultrastructural observations

23 December 2023

113

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A mutation in the mucosal keratin K4 is associated with oral white sponge nevus

23 December 2023

114

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Keratin 13 point mutation underlies the hereditary mucosal epithelial disorder white sponge nevus

23 December 2023

115

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A glutamine insertion in the 1A alpha helical domain of the keratin 4 gene in a familial case of white sponge nevus

23 December 2023

116

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A novel mutation in the keratin 13 gene causing oral white sponge nevus

23 December 2023

117

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Identification of two novel mutations in keratin 13 as the cause of white sponge naevus.

23 December 2023

118

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Cornea-specific expression of K12 keratin during mouse development.

23 December 2023

122

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Investigative Ophthalmology Visual Science

23 December 2023

123

37

2572

Kao

1996

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy

23 December 2023

124

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy

23 December 2023

125

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A novel mutation in the helix termination motif of keratin K12 in a US family with Meesmann corneal dystrophy

23 December 2023

126

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Molecular genetics of Meesmann's corneal dystrophy: ancestral and novel mutations in keratin 12 (K12) and complete sequence of the human KRT12 gene.

23 December 2023

127

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy

23 December 2023

128

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Chronic hepatitis, hepatocyte fragility, and increased soluble phosphoglycokeratins in transgenic mice expressing a keratin 18 conserved arginine mutant

23 December 2023

129

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Mutation of human keratin 18 in association with cryptogenic cirrhosis

23 December 2023

130

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Keratin 8 mutations in patients with cryptogenic liver disease

23 December 2023

131

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Pathogenesis of monilethrix: computer stereography and electron microscopy

23 December 2023

132

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13

23 December 2023

133

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Linkage of monilethrix to the trichocyte and epithelial keratin gene cluster on 12q11-q13

23 December 2023

134

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix

23 December 2023

135

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix

23 December 2023

136

1 reference

https://api.crossref.org/works/10.2165/00128071-200304050-00005

Cloning and characterization of multiple human genes and cDNAs encoding highly related type II keratin 6 isoforms

23 December 2023

137

1 reference

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Molecular Biology and Evolution

23 December 2023

138

5

97

Savtchenko

1988

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140

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141

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142

1 reference

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A mutation detection strategy for the human keratin 6A gene and novel missense mutations in two cases of pachyonychia congenita type 1

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143

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144

1 reference

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Plectin and human genetic disorders of the skin and muscle. The paradigm of epidermolysis bullosa with muscular dystrophy

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145

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Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome

23 December 2023

146

1 reference

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147

1 reference

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Prenatal diagnosis of epidermolytic hyperkeratosis by direct gene sequencing

23 December 2023

148

1 reference

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Prenatal diagnosis for keratin mutations to exclude transmission of epidermolytic hyperkeratosis

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149

1 reference

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23 December 2023

Identifiers

1 reference

Dimensions Publication ID

31 July 2017

1015148457

0 references

1 reference