Characteristics of Clinical and Electrophysiological Pattern in a Large Cohort of Chinese Patients With Charcot-Marie-Tooth 4C

The “Src homology 3 (SH3) domain and tetratricopeptide repeats 2” (SH3TC2) gene is mutated in individuals with Charcot-Marie-Tooth disease (CMT) and considered relevant to a demyelinating or intermediate subtype of CMT disease, CMT4C. In this study, we screened a cohort of 465 unrelated Chinese CMT...

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Detalles Bibliográficos
Autores principales: Duan, Xiaohui, Ma, Yan, Fan, Dongsheng, Liu, Xiaoxuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907161/
https://www.ncbi.nlm.nih.gov/pubmed/33643188
http://dx.doi.org/10.3389/fneur.2021.598168

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7907161/
https://www.ncbi.nlm.nih.gov/pubmed/33643188
http://dx.doi.org/10.3389/fneur.2021.598168

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