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Simvastatin offers new prospects for the treatment of Duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD) is the most common and severe inherited neuromuscular disorder. DMD is caused by mutations in the gene encoding the dystrophin protein in muscle fibers. Dystrophin was originally proposed to be a structural protein that protected the sarcolemma from stresses produce...
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| Опубликовано в: : | Rare Dis |
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| Главные авторы: | , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Taylor & Francis
2016
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4838314/ https://ncbi.nlm.nih.gov/pubmed/27141415 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/21675511.2016.1156286 |
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