Disease Phenotypes and Mechanisms of iPSC-Derived Cardiomyocytes From Brugada Syndrome Patients With a Loss-of-Function SCN5A Mutation
2020 | journal article. A publication with affiliation to the University of Göttingen.
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Cite this publication
Li W, Stauske M, Luo X, Wagner S, Vollrath M, Mehnert CS, et al. Disease Phenotypes and Mechanisms of iPSC-Derived Cardiomyocytes From Brugada Syndrome Patients With a Loss-of-Function SCN5A Mutation. Frontiers in Cell and Developmental Biology. 2020;8. doi:10.3389/fcell.2020.592893.
Documents & Media
Details
- Authors
- 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
- Issue Date
- 2020
- Journal
- Frontiers in Cell and Developmental Biology
- eISSN
- 2296-634X
