Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies (Q24633171)

2

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Alana S Golden

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Bruce L Tempel

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Thomas D Bird

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Phillip F Chance

American Journal of Human Genetics

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language of work or name

English

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publication date

January 2002

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published in

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volume

70

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issue

1

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page(s)

244-50

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cites work

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A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene

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N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom

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BAR: An apoptosis regulator at the intersection of caspases and Bcl-2 family proteins

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Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies

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A comprehensive genetic map of the human genome based on 5,264 microsatellites

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Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

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Peripheral demyelination and neuropathic pain behavior in periaxin-deficient mice

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Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

7 April 2017

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Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E.

7 April 2017

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A mutation in periaxin is responsible for CMT4F, an autosomal recessive form of Charcot-Marie-Tooth disease

27 September 2017

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Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2.

27 September 2017

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Rho-dependent regulation of cell spreading by the tetraspan membrane protein Gas3/PMP22.

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Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3.

27 September 2017

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Charcot-Marie-Tooth disease: lessons in genetic mechanisms

27 September 2017

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Epithelial membrane protein-2 and epithelial membrane protein-3: two novel members of the peripheral myelin protein 22 gene family

27 September 2017

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Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.

27 September 2017

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Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication

27 September 2017

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Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies

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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

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Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A.

27 September 2017

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A case of congenital hypomyelination neuropathy. Clinical, morphological, and chemical studies

27 September 2017

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The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A

27 September 2017

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

30 May 2018

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

28 July 2018

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The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication

28 November 2018

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

28 November 2018

1 reference

12 December 2020

Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locus

1 reference

12 December 2020

The peripheral myelin gene PMP-22/GAS-3 is duplicated in Charcot-Marie-Tooth disease type 1A

1 reference

12 December 2020

Ultrastructural study of a nerve biopsy from a case of early infantile chronic neuropathy

1 reference

12 December 2020

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

1 reference

12 December 2020

A routine method for the establishment of permanent growing lymphoblastoid cell lines

1 reference

12 December 2020

Identification of a 5' splice site mutation in the PMP-22 gene in autosomal dominant Charcot-Marie-Tooth disease type 1

1 reference

12 December 2020

Absence of PMP22 coding region mutations in CMT1A duplication patients: further evidence supporting gene dosage as a mechanism for Charcot-Marie-Tooth disease type 1A

1 reference

12 December 2020

Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)

1 reference

12 December 2020