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X-linked Charcot-Marie-Tooth disease
The X-linked form of Charcot-Marie-Tooth disease (CMT1X) is the second most common form of hereditary motor and sensory neuropathy. The clinical phenotype is characterized by progressive muscle atrophy and weakness, areflexia, and variable sensory abnormalities; central nervous system manifestations...
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| Main Authors: | , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2012
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3779456/ https://ncbi.nlm.nih.gov/pubmed/23279425 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1529-8027.2012.00424.x |
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