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Pharmacologic Management of Duchenne Muscular Dystrophy: Target Identification and Preclinical Trials
Duchenne muscular dystrophy (DMD) is an X-linked human disorder in which absence of the protein dystrophin causes degeneration of skeletal and cardiac muscle. For the sake of treatment development, over and above definitive genetic and cell-based therapies, there is considerable interest in drugs th...
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| Auteurs principaux: | , , , , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Oxford University Press
2014
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4158345/ https://ncbi.nlm.nih.gov/pubmed/24936034 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ilar/ilu011 |
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