SCN5A gene variants and arrhythmic risk in Brugada Syndrome: an updated systematic review and meta-analysis

A rare gene variant in SCN5A can be found in approximately 20-25% of patients with Brugada syndrome (BrS).

Source: Heart Rhythm - April 10, 2024 Category: Cardiology Authors: Ioannis Doundoulakis, Luigi Pannone, Sotirios Chiotis, Domenico Giovanni Della Rocca, Antonio Sorgente, Panagiotis Tsioufis, Alvise Del Monte, Giampaolo Vetta, Christos Piperis, Ingrid Overeinder, Gezim Bala, Alexandre Almorad, Erwin Str öker, Juan Sieir Source Type: research