Brugada Syndrome: Different Experimental Models and the Role of Human Cardiomyocytes From Induced Pluripotent Stem Cells

Brugada syndrome (BrS) is an inherited and rare cardiac arrhythmogenic disease associated with an increased risk of ventricular fibrillation and sudden cardiac death. Different genes have been linked to BrS. The majority of mutations are located in the SCN5A gene, and the typical abnormal ECG is an...

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Detalles Bibliográficos
Autores principales: Li, Yingrui, Lang, Siegfried, Akin, Ibrahim, Zhou, Xiaobo, El‐Battrawy, Ibrahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Contemporary Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075459/
https://www.ncbi.nlm.nih.gov/pubmed/35322667
http://dx.doi.org/10.1161/JAHA.121.024410

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075459/
https://www.ncbi.nlm.nih.gov/pubmed/35322667
http://dx.doi.org/10.1161/JAHA.121.024410

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