Advances in Stem Cell Modeling of Dystrophin-Associated Disease: Implications for the Wider World of Dilated Cardiomyopathy

Familial dilated cardiomyopathy (DCM) is mostly caused by mutations in genes encoding cytoskeletal and sarcomeric proteins. In the pediatric population, DCM is the predominant type of primitive myocardial disease. A severe form of DCM is associated with mutations in the DMD gene encoding dystrophin,...

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Detalhes bibliográficos
Publicado no:Front Physiol
Main Authors: Pioner, Josè Manuel, Fornaro, Alessandra, Coppini, Raffaele, Ceschia, Nicole, Sacconi, Leonardo, Donati, Maria Alice, Favilli, Silvia, Poggesi, Corrado, Olivotto, Iacopo, Ferrantini, Cecilia
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2020
Assuntos:
Physiology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7235370/
https://ncbi.nlm.nih.gov/pubmed/32477154
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2020.00368
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