Studying Brugada Syndrome With an SCN1B Variants in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes

BACKGROUND: Among rare channelopathies BrS patients are at high risk of sudden cardiac death (SCD). SCN5A mutations are found in a quarter of patients. Other rare gene mutations including SCN1B have been implicated to BrS. Studying the human cellular phenotype of BrS associated with rare gene mutati...

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Detalles Bibliográficos
Autores principales: El-Battrawy, Ibrahim, Müller, Jonas, Zhao, Zhihan, Cyganek, Lukas, Zhong, Rujia, Zhang, Feng, Kleinsorge, Mandy, Lan, Huan, Li, Xin, Xu, Qiang, Huang, Mengying, Liao, Zhenxing, Moscu-Gregor, Alexander, Albers, Sebastian, Dinkel, Hendrik, Lang, Siegfried, Diecke, Sebastian, Zimmermann, Wolfram-Hubertus, Utikal, Jochen, Wieland, Thomas, Borggrefe, Martin, Zhou, Xiaobo, Akin, Ibrahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839339/
https://www.ncbi.nlm.nih.gov/pubmed/31737628
http://dx.doi.org/10.3389/fcell.2019.00261

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6839339/
https://www.ncbi.nlm.nih.gov/pubmed/31737628
http://dx.doi.org/10.3389/fcell.2019.00261

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