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DMD carrier model with mosaic dystrophin expression in the heart reveals complex vulnerability to myocardial injury
Duchenne muscular dystrophy (DMD) is a devastating neuromuscular disease that causes progressive muscle wasting and cardiomyopathy. This X-linked disease results from mutations of the DMD allele on the X-chromosome resulting in the loss of expression of the protein dystrophin. Dystrophin loss causes...
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| Publicat a: | Hum Mol Genet |
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| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2020
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7158376/ https://ncbi.nlm.nih.gov/pubmed/31976522 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddaa015 |
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