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Calpain 3 deficiency affects SERCA expression and function in the skeletal muscle
Limb-girdle muscular dystrophy type 2A (LGMD2A) is a form of muscular dystrophy caused by mutations in calpain 3 (CAPN3). Several studies have implicated Ca(2+) dysregulation as an underlying event in several muscular dystrophies, including LGMD2A. In this study we used mouse and human myotube cultu...
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| Publicado no: | Expert Rev Mol Med |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Cambridge University Press
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4836212/ https://ncbi.nlm.nih.gov/pubmed/27055500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/erm.2016.9 |
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