Investigating the cardiac pathology of SCO2‐mediated hypertrophic cardiomyopathy using patients induced pluripotent stem cell–derived cardiomyocytes

Mutations in SCO2 are among the most common causes of COX deficiency, resulting in reduced mitochondrial oxidative ATP production capacity, often leading to hypertrophic cardiomyopathy (HCM). To date, none of the recent pertaining reports provide deep understanding of the SCO2 disease pathophysiolog...

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Bibliografski detalji
Izdano u:J Cell Mol Med
Glavni autori: Hallas, Tova, Eisen, Binyamin, Shemer, Yuval, Ben Jehuda, Ronen, Mekies, Lucy N., Naor, Shulamit, Schick, Revital, Eliyahu, Sivan, Reiter, Irina, Vlodavsky, Eugene, Katz, Yeshayahu (Shai), Õunap, Katrin, Lorber, Avraham, Rodenburg, Richard, Mandel, Hanna, Gherghiceanu, Mihaela, Binah, Ofer
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2017
Teme:
Original Articles
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC5783844/
https://ncbi.nlm.nih.gov/pubmed/29193756
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.13392
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