Advances in Stem Cell Modeling of Dystrophin-Associated Disease: Implications for the Wider World of Dilated Cardiomyopathy.
dilated cardiomyopathy (DCM)
duchenne muscular dystrophy (DMD)
dystrophin (DMD)
hiPSC-cardiomyocyte
stem cell models
Journal
Frontiers in physiology
ISSN: 1664-042X
Titre abrégé: Front Physiol
Pays: Switzerland
ID NLM: 101549006
Informations de publication
Date de publication:
2020
2020
Historique:
received:
20
01
2020
accepted:
30
03
2020
entrez:
2
6
2020
pubmed:
2
6
2020
medline:
2
6
2020
Statut:
epublish
Résumé
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
Identifiants
pubmed: 32477154
doi: 10.3389/fphys.2020.00368
pmc: PMC7235370
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
368Informations de copyright
Copyright © 2020 Pioner, Fornaro, Coppini, Ceschia, Sacconi, Donati, Favilli, Poggesi, Olivotto and Ferrantini.
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