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Emerging strategies for cell and gene therapy of the muscular dystrophies
The muscular dystrophies are a heterogeneous group of over 40 disorders that are characterised by muscle weakness and wasting. The most common are Duchenne muscular dystrophy and Becker muscular dystrophy, which result from mutations within the gene encoding dystrophin; myotonic dystrophy type 1, wh...
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| Pubblicato in: | Expert Rev Mol Med |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2009
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4890545/ https://ncbi.nlm.nih.gov/pubmed/19555515 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1017/S1462399409001100 |
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