Brugada syndrome: A comprehensive review of pathophysiological mechanisms and risk stratification strategies

Brugada syndrome (BrS) is an inherited ion channel channelopathy predisposing to ventricular arrhythmias and sudden cardiac death. Originally believed to be predominantly associated with mutations in SCN5A encoding for the cardiac sodium channel, mutations of 18 genes other than SCN5A have been impl...

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Detalles Bibliográficos
Autores principales: Li, Ka Hou Christien, Lee, Sharen, Yin, Chengye, Liu, Tong, Ngarmukos, Tachapong, Conte, Giulio, Yan, Gan-Xin, Sy, Raymond W., Letsas, Konstantinos P., Tse, Gary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974766/
https://www.ncbi.nlm.nih.gov/pubmed/31993492
http://dx.doi.org/10.1016/j.ijcha.2020.100468

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974766/
https://www.ncbi.nlm.nih.gov/pubmed/31993492
http://dx.doi.org/10.1016/j.ijcha.2020.100468

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