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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Vydáno v:Front Physiol
Hlavní autoři: Pioner, Josè Manuel, Fornaro, Alessandra, Coppini, Raffaele, Ceschia, Nicole, Sacconi, Leonardo, Donati, Maria Alice, Favilli, Silvia, Poggesi, Corrado, Olivotto, Iacopo, Ferrantini, Cecilia
Médium: Artigo
Jazyk:Inglês
Vydáno: Frontiers Media S.A. 2020
Témata:
Physiology
On-line přístup: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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