Myelin protein zero gene mutated in Charcot-Marie-tooth type 1B patients (Q24564085)

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D G Brooks

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L Li

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J Lepercq

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J A Trofatter

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J V Ravetch

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R V Lebo

Proceedings of the National Academy of Sciences of the United States of America

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language of work or name

English

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publication date

15 November 1993

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published in

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volume

90

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issue

22

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page(s)

10856-60

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cites work

Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47877

Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene

24 March 2017

1 reference

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Organization of the human and mouse low-affinity Fc gamma R genes: duplication and recombination

24 March 2017

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Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin

24 March 2017

1 reference

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Construction of a physical map on mouse and human chromosome 1: comparison of 13 Mb of mouse and 11 Mb of human DNA

24 March 2017

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Evidence for linkage of Charcot-Marie-Tooth neuropathy to the Duffy locus on chromosome 1.

24 March 2017

1 reference

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Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).

27 September 2017

1 reference

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Multicolor in situ hybridization and linkage analysis order Charcot-Marie-Tooth type I (CMTIA) gene-region markers

27 September 2017

1 reference

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Comparative studies on myelin proteins in mammalian peripheral nerve

27 September 2017

1 reference

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Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathy

27 September 2017

1 reference

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Myelin Po‐protein, more than just a structural protein?

27 September 2017

1 reference

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Expressing antisense P0 RNA in Schwann cells perturbs myelination

27 September 2017

1 reference

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DNA Sequence, genomic organization, and chromosomal localization of the mouse peripheral myelin protein zero gene: Identification of polymorphic alleles

30 May 2018

1 reference

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Multicolor fluorescence in situ hybridization and pulsed field electrophoresis dissect CMT1B gene region

30 May 2018

1 reference

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Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc? receptor gene region

30 May 2018

1 reference

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Regional assignment of the human keratin 5 (KRT5) gene to chromosome 12q near D12S14 by PCR analysis of somatic cell hybrids and multicolor in situ hybridization

30 May 2018

1 reference

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Proposed nomenclature for PNS myelin proteins

30 May 2018

1 reference

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Identical point mutations of PMP-22 in Trembler-J mouse and Charcot-Marie-Tooth disease type 1A

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47877

Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47877

Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A by multicolor in situ hybridization

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47877

X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=47877

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. II. Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations

28 November 2018

1 reference

12 December 2020

Dominantly inherited peroneal muscular atrophy (hereditary motor and sensory neuropathy type I) in infancy and childhood

1 reference

12 December 2020

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17

1 reference

12 December 2020

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

12 December 2020

Genetic and clinical aspects of Charcot-Marie-Tooth's disease

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.90.22.10856

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ADS bibcode

1993PNAS...9010856S

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1 reference

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PubMed publication ID

7504284

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