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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Dades bibliogràfiques
Publicat a:J Arrhythm
Autors principals: Raharjo, Sunu Budhi, Maulana, Rido, Maghfirah, Irma, Alzahra, Fatimah, Putrinarita, Agnes Dinar, Hanafy, Dicky A., Yuniadi, Yoga
Format: Artigo
Idioma:Inglês
Publicat: John Wiley and Sons Inc. 2018
Matèries:
Clinical Reviews
Accés en línia: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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