SCN5A gene mutations and the risk of ventricular fibrillation and syncope in Brugada syndrome patients: A meta‐analysis
Abstract 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‐analy...
Main Authors: | Sunu Budhi Raharjo, Rido Maulana, Irma Maghfirah, Fatimah Alzahra, Agnes Dinar Putrinarita, Dicky A. Hanafy, Yoga Yuniadi |
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Format: | Article |
Language: | English |
Published: |
Wiley
2018-10-01
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Series: | Journal of Arrhythmia |
Subjects: | |
Online Access: | https://doi.org/10.1002/joa3.12097 |
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