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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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Arrhythm
Prif Awduron: Raharjo, Sunu Budhi, Maulana, Rido, Maghfirah, Irma, Alzahra, Fatimah, Putrinarita, Agnes Dinar, Hanafy, Dicky A., Yuniadi, Yoga
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: John Wiley and Sons Inc. 2018
Pynciau:
Clinical Reviews
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6174414/
https://ncbi.nlm.nih.gov/pubmed/30327691
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/joa3.12097
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