Učitavanje...
Emerging genetic therapies to treat Duchenne muscular dystrophy
PURPOSE OF REVIEW: Duchenne muscular dystrophy is a progressive muscle degenerative disease caused by dystrophin mutations. The purpose of this review is to highlight two emerging therapies designed to repair the primary genetic defect, called `exon skipping' and `nonsense codon suppression...
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| Glavni autori: | , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2009
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2856442/ https://ncbi.nlm.nih.gov/pubmed/19745732 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WCO.0b013e32832fd487 |
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