Clinical and Pathological Variation of Charcot-Marie-Tooth 1A in a Large Chinese Cohort

Charcot-Marie-Tooth 1A (CMT1A) caused by peripheral myelin protein 22 (PMP22) gene duplication is the most common form of hereditary polyneuropathy. Twenty-four genetically confirmed CMT1A patients with sural nerve biopsies were enrolled in this study. The clinical picture included a great variabili...

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Detalles Bibliográficos
Autores principales: Wu, Rui, Lv, He, Zhang, Wei, Wang, Zhaoxia, Zuo, Yuehuan, Liu, Jing, Yuan, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556987/
https://www.ncbi.nlm.nih.gov/pubmed/28835897
http://dx.doi.org/10.1155/2017/6481367

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556987/
https://www.ncbi.nlm.nih.gov/pubmed/28835897
http://dx.doi.org/10.1155/2017/6481367

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