Associated Papers
A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand.
Walsh R et al.
Circulation, 2025
39391988 (PubMed )
Supplement: cir-151-31-s003.xlsx › Table_S3
Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review.
Oliva A et al.
Journal of Clinical Medicine, 2022
Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome.
Nademanee K et al.
Journal of the American College of Cardiology, 2015
Age, Genetics, and Fibrosis in the Brugada Syndrome.
Campuzano O et al.
Journal of the American College of Cardiology, 2015
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