GDAP1 mutations in Czech families with early-onset CMT-Reference-Cited by-同舟云学术

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GDAP1 mutations in Czech families with early-onset CMT

Published:2007-06 Issue:6 Volume:17 Page:482-489
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Baránková L.,Vyhnálková E.,Züchner S.,Mazanec R.,Sakmaryová I.,Vondráček P.,Merlini L.,Bojar M.,Nelis E.,De Jonghe P.,Seeman P.

Publisher

Elsevier BV

Subject

Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health

Reference17 articles.

1. Hereditary motor and sensory neuropathies;Dyck,1993

2. The clinical features of hereditary motor and sensory neuropathy types I and II;Harding;Brain,1980

3. Classification of the hereditary motor and sensory neuropathies;Reilly;Curr Opin Neurol,2000

4. Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21;Baxter;Nat Genet,2002

5. The gene encoding ganglioside-induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease;Cuesta;Nat Genet,2002

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1. The Spectrum of Disease-Associated Alleles in Countries with a Predominantly Slavic Population;International Journal of Molecular Sciences;2024-08-28

2. Hereditary neuropathies in childhood;Neurologie pro praxi;2022-03-14

3. Impaired Mitochondrial Mobility in Charcot-Marie-Tooth Disease;Frontiers in Cell and Developmental Biology;2021-02-01

4. Clinical and genetic investigation in Chinese patients with demyelinating Charcot‐Marie‐Tooth disease;Journal of the Peripheral Nervous System;2018-09-24

5. Genotype–phenotype correlation and frequency of distribution in a cohort of Chinese Charcot–Marie–Tooth patients associated with GDAP1 mutations;Journal of Neurology;2018-01-25

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