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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...

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Bibliografski detalji
Izdano u:Ann Clin Transl Neurol
Glavni autori: Hsu, Yun‐Hsin, Lin, Kon‐Ping, Guo, Yuh‐Cherng, Tsai, Yu‐Shuen, Liao, Yi‐Chu, Lee, Yi‐Chung
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2019
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6562034/
https://ncbi.nlm.nih.gov/pubmed/31211173
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/acn3.50797
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