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Disease Phenotypes and Mechanisms of iPSC-Derived Cardiomyocytes From Brugada Syndrome Patients With a Loss-of-Function SCN5A Mutation

Wener Li, Michael Stauske, Xiaojing Luo, Stefan Wagner, Meike Vollrath, Carola S. Mehnert, Mario Schubert, Lukas Cyganek, Simin Chen, Sayed-Mohammad Hasheminasab, Gerald Wulf, Ali El‐Armouche, Lars S. Maier, Gerd Hasenfuß, Kaomei Guan

2020Frontiers in Cell and Developmental Biology37 citationsDOIOpen Access PDF

Abstract

in BrS-CMs and alleviated the arrhythmic activity, suggesting their therapeutic potential for BrS patients.

Topics & Concepts

Brugada syndromeRepolarizationPhenotypeSudden cardiac deathInternal medicineMedicineInduced pluripotent stem cellSudden deathElectrophysiologyMutationCilostazolNerve conduction velocityConnexinCardiologyEndocrinologyCell biologyBiologyGap junctionIntracellularGeneticsGeneEmbryonic stem cellAspirinCardiac electrophysiology and arrhythmiasIon channel regulation and functionNeuroscience and Neural Engineering
Disease Phenotypes and Mechanisms of iPSC-Derived Cardiomyocytes From Brugada Syndrome Patients With a Loss-of-Function SCN5A Mutation | Litcius