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The genetics of Charcot–Marie–Tooth disease: current trends and future implications for diagnosis and management
Charcot–Marie–Tooth (CMT) disease is the most common hereditary polyneuropathy and is classically associated with an insidious onset of distal predominant motor and sensory loss, muscle wasting, and pes cavus. Other forms of hereditary neuropathy, including sensory predominant or motor predominant f...
Tallennettuna:
| Julkaisussa: | Appl Clin Genet |
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| Päätekijät: | , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Dove Medical Press
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4621202/ https://ncbi.nlm.nih.gov/pubmed/26527893 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/TACG.S69969 |
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