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Clinical and Genetic Features of Chinese X-linked Charcot-Marie-Tooth Type 1 Disease
BACKGROUND: X-linked Charcot-Marie-Tooth type 1 (CMT1X) disease is one of the most common forms of inherited neuropathy caused by mutations in the gap junction beta-1 protein (GJB1) gene (also known as connexin 32). This study presented the clinical and genetic features of a series of Chinese patien...
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| Publicado no: | Chin Med J (Engl) |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5421174/ https://ncbi.nlm.nih.gov/pubmed/28469099 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0366-6999.204925 |
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