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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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| Vydáno v: | Rare Dis |
|---|---|
| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Taylor & Francis
2016
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| Témata: | |
| On-line přístup: | 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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