Brugada syndrome: a fatal disease with complex genetic etiologies – still a long way to go

Brugada syndrome (BrS) is an arrhythmogenic disorder which was first described in 1992. This disease is a channelopathy characterized by ST-segment elevations in the right precordial leads and is susceptible to sudden death. BrS is a fatal disease with gender and age preferences. It occurs mainly in...

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Detalles Bibliográficos
Autores principales: Wu, Yeda, Ai, Mei, Bardeesi, Adham Sameer A., Xu, Lunwu, Zheng, Jingjing, Zheng, Da, Yin, Kun, Wu, Qiuping, Zhang, Liyong, Huang, Lei, Cheng, Jianding
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Authoritative Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197104/
https://www.ncbi.nlm.nih.gov/pubmed/30483629
http://dx.doi.org/10.1080/20961790.2017.1333203

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197104/
https://www.ncbi.nlm.nih.gov/pubmed/30483629
http://dx.doi.org/10.1080/20961790.2017.1333203

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