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Calpain 3 is a modulator of the dysferlin protein complex in skeletal muscle
Muscular dystrophies comprise a genetically heterogeneous group of degenerative muscle disorders characterized by progressive muscle wasting and weakness. Two forms of limb-girdle muscular dystrophy, 2A and 2B, are caused by mutations in calpain 3 (CAPN3) and dysferlin (DYSF), respectively. While CA...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2900895/ https://ncbi.nlm.nih.gov/pubmed/18334579 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn081 |
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