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.
Jump to: Cite & Linked | Documents & Media | Details | Version history
Cite this publication
Li, Wener, Michael Stauske, Xiaojing Luo, Stefan Wagner, Meike Vollrath, Carola S. Mehnert, Mario Schubert 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 8 (2020): . https://doi.org/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