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Emerging gene editing strategies for Duchenne muscular dystrophy targeting stem cells
The progressive loss of muscle mass characteristic of many muscular dystrophies impairs the efficacy of most of the gene and molecular therapies currently being pursued for the treatment of those disorders. It is becoming increasingly evident that a therapeutic application, to be effective, needs to...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2014
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4001063/ https://ncbi.nlm.nih.gov/pubmed/24795643 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2014.00148 |
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