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Molecular Genetics of Charcot-Marie-Tooth Disease: From Genes to Genomes
Charcot-Marie-Tooth disease (CMT) is a heterogeneous group of disorders of the peripheral nervous system, mainly characterized by distal muscle weakness and atrophy leading to motor handicap. With an estimated prevalence of 1 in 2,500, this condition is one of the most commonly inherited neurologica...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
S. Karger AG
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3531925/ https://ncbi.nlm.nih.gov/pubmed/23293578 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000343487 |
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