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Intermediate Charcot-Marie-Tooth disease
Charcot-Marie-Tooth (CMT) disease is a common neurogenetic disorder and its heterogeneity is a challenge for genetic diagnostics. The genetic diagnostic procedures for a CMT patient can be explored according to the electrophysiological criteria: very slow motor nerve conduction velocity (MNCV) (<...
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| Yayımlandı: | Neurosci Bull |
|---|---|
| Asıl Yazarlar: | , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences
2014
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5562560/ https://ncbi.nlm.nih.gov/pubmed/25326399 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12264-014-1475-7 |
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