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Clinical and Pathological Variation of Charcot-Marie-Tooth 1A in a Large Chinese Cohort
Charcot-Marie-Tooth 1A (CMT1A) caused by peripheral myelin protein 22 (PMP22) gene duplication is the most common form of hereditary polyneuropathy. Twenty-four genetically confirmed CMT1A patients with sural nerve biopsies were enrolled in this study. The clinical picture included a great variabili...
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| Pubblicato in: | Biomed Res Int |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Hindawi
2017
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5556987/ https://ncbi.nlm.nih.gov/pubmed/28835897 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/6481367 |
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