A novel PMP22 insertion mutation causing Charcot–Marie–Tooth disease type 3-Reference-Cited by-同舟云学术

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A novel PMP22 insertion mutation causing Charcot–Marie–Tooth disease type 3

Published:2021-03-19 Issue:11 Volume:100 Page:e25163
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Han Liang,Huang Yanjing,Nie Yuan,Li Jing,Chen Gang,Tu Shenghao,Shen Pan,Chen Chao

Funder

National Natural Science Foundation of China

Natural Science Foundation of Hubei Province

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference32 articles.

1. Diagnosis, natural history, and management of Charcot–Marie–Tooth disease;Pareyson;Lancet Neurol,2009

2. Dejerine–Sottas syndrome grown to maturity: overview of genetic and morphological heterogeneity and follow-up of 25 patients;Gabreels-Festen;J Anat,2002

3. Schwann cell and the pathogenesis of Charcot–Marie–Tooth disease;Murakami;Adv Exp Med Biol,2019

4. Clinical and genetic aspects of Charcot–Marie–Tooth disease subtypes;Nam;Precis Future Med,2019

5. SWISS-MODEL: homology modelling of protein structures and complexes;Waterhouse;Nucleic Acids Res,2018

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1. Facilitations and Hurdles of Genetic Testing in Neuromuscular Disorders;Diagnostics;2021-04-14

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