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Targeting Fibrosis in Duchenne Muscular Dystrophy
Duchenne muscular dystrophy (DMD) is the most common genetic muscle disease affecting 1 in 3,500 live male births. It is an X-linked recessive disease caused by a defective dystrophin gene. The disease is characterized by progressive limb weakness, respiratory and cardiac failure and premature death...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2916968/ https://ncbi.nlm.nih.gov/pubmed/20613637 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/NEN.0b013e3181e9a34b |
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