Article

p.D372H: A novel SCN5A mutation associated with Brugada syndrome

2025-02-01

Abstract excerpt

<h4>Background</h4> Brugada syndrome (BrS) is a genetic cardiac arrhythmia disorder inherited in an autosomal dominant manner, characterized by ST-segment elevation in the right precordial leads (V1-V3) on electrocardiograms (ECGs). This syndrome predominantly affects young individuals with structurally normal hearts and significantly increases the risk of ventricular arrhythmias and sudden cardiac death (SCD). T...

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Literature Corpus work: 2d703474-2a08-54ec-8fcc-af9adfb5c52b
DOI: 10.1101/2025.01.29.635599

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