SCN5A mutation status increases the risk of major arrhythmic events in Asian populations with Brugada syndrome: systematic review and meta‐analysis

BACKGROUND: Brugada syndrome (BrS) is an inherited arrhythmic disease linked to SCN5A mutations. It is controversial whether SCN5A mutation carriers possess a greater risk of major arrhythmic events (MAE). We examined the association of SCN5A mutations and MAE in BrS patients. METHODS: We comprehens...

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Detalhes bibliográficos
Publicado no:Ann Noninvasive Electrocardiol
Main Authors: Rattanawong, Pattara, Chenbhanich, Jirat, Mekraksakit, Poemlarp, Vutthikraivit, Wasawat, Chongsathidkiet, Pakawat, Limpruttidham, Nath, Prasitlumkum, Narut, Chung, Eugene H.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2018
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6931443/
https://ncbi.nlm.nih.gov/pubmed/30126015
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/anec.12589
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