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miR-31 modulates dystrophin expression: new implications for Duchenne muscular dystrophy therapy
Duchenne muscular dystrophy (DMD)—which is caused by mutations in the dystrophin gene—is one of the most severe myopathies. Among therapeutic strategies, exon skipping allows the rescue of dystrophin synthesis through the production of a shorter but functional messenger RNA. Here, we report the iden...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3049433/ https://ncbi.nlm.nih.gov/pubmed/21212803 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/embor.2010.208 |
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