Mutation spectrum of Charcot‐Marie‐Tooth disease among the Han Chinese in Taiwan

OBJECTIVE: Charcot‐Marie‐Tooth disease (CMT) is a clinically and genetically heterogeneous group of inherited neuropathies. Mutations in more than 90 genes have been implicated in CMT; however, the mutational spectrum of CMT in Chinese population remains obscure. This study aims to provide a compreh...

Descripción completa

Detalles Bibliográficos
Autores principales: Hsu, Yun‐Hsin, Lin, Kon‐Ping, Guo, Yuh‐Cherng, Tsai, Yu‐Shuen, Liao, Yi‐Chu, Lee, Yi‐Chung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562034/
https://www.ncbi.nlm.nih.gov/pubmed/31211173
http://dx.doi.org/10.1002/acn3.50797

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562034/
https://www.ncbi.nlm.nih.gov/pubmed/31211173
http://dx.doi.org/10.1002/acn3.50797

Ejemplares similares