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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
John Wiley and Sons Inc.
2019
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| Materias: | |
| 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 |