Comprehensive interpretation of genes associated with Brugada Syndrome (an inherited arrhythmogenic disease associated with sudden cardiac death) and identify only several with a conclusive pathogenic role via @WileyGenetics https://t.co/aokHSgJIOe
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RT @DrJTriasDeBes: Beyond SCN5A, the authors conclude definitive pathogenic variants associated with Brugada syndrome in four minor genes.…
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Beyond SCN5A, the authors conclude definitive pathogenic variants associated with Brugada syndrome in four minor genes. The current list of genes associated with BrS therefore should include SCN5A, SLMAP, SEMA3A, SCNN1A, and SCN2B. https://t.co/b7QVHN9FX