SCN5A gene mutations and the risk of ventricular fibrillation and syncope in Brugada syndrome patients: A meta‐analysis

Mutations in the gene encoding the main cardiac sodium channel (SCN5A) are the commonest genetic cause of Brugada syndrome (BrS). However, the effect of SCN5A mutations on the outcomes of ventricular fibrillation (VF) and syncope remains uncertain. To clarify this relationship, a meta‐analysis was p...

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Detalles Bibliográficos
Autores principales: Raharjo, Sunu Budhi, Maulana, Rido, Maghfirah, Irma, Alzahra, Fatimah, Putrinarita, Agnes Dinar, Hanafy, Dicky A., Yuniadi, Yoga
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Clinical Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174414/
https://www.ncbi.nlm.nih.gov/pubmed/30327691
http://dx.doi.org/10.1002/joa3.12097

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174414/
https://www.ncbi.nlm.nih.gov/pubmed/30327691
http://dx.doi.org/10.1002/joa3.12097

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