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Duchenne muscular dystrophy mice and men: Can understanding a genetic cardiomyopathy inform treatment of other myocardial diseases?

Duchenne muscular dystrophy (DMD) mouse models have a predictable and reproducible time-course of cardiomyopathy progression with discrete pathogenic steps, which closely parallel what we know occurs in the cardiomyopathy of patients with DMD. The slow progression of early pathogenic steps common to...

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Detalles Bibliográficos
Publicado en:Circ Res
Main Authors: Rafael-Fortney, Jill A., Chadwick, Jessica A., Raman, Subha V.
Formato: Artigo
Idioma:Inglês
Publicado: 2016
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4819164/
https://ncbi.nlm.nih.gov/pubmed/27034274
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCRESAHA.116.308402
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