Disease Phenotypes and Mechanisms of iPSC-Derived Cardiomyocytes From Brugada Syndrome Patients With a Loss-of-Function SCN5A Mutation-Reference-Cited by-同舟云学术

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

Published:2020-10-22 Issue: Volume:8 Page:
ISSN:2296-634X
Container-title:Frontiers in Cell and Developmental Biology
language:
Short-container-title:Front. Cell Dev. Biol.

Author:

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

Publisher

Frontiers Media SA

Subject

Cell Biology,Developmental Biology

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