Functional abnormalities in iPSC-derived cardiomyocytes generated from CPVT1 and CPVT2 patients carrying ryanodine or calsequestrin mutations

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmia characterized by syncope and sudden death occurring during exercise or acute emotion. CPVT is caused by abnormal intracellular Ca(2+) handling resulting from mutations in the RyR2 or CASQ2 genes. Because CASQ2 an...

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Detalhes bibliográficos
Publicado no:J Cell Mol Med
Main Authors: Novak, Atara, Barad, Lili, Lorber, Avraham, Gherghiceanu, Mihaela, Reiter, Irina, Eisen, Binyamin, Eldor, Liron, Itskovitz-Eldor, Joseph, Eldar, Michael, Arad, Michael, Binah, Ofer
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley & Sons, Ltd 2015
Assuntos:
Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4549051/
https://ncbi.nlm.nih.gov/pubmed/26153920
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.12581
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