Multiple arrhythmic syndromes in a newborn, owing to a novel mutation in SCN5A.

Abstract

BACKGROUND Mutations in the SCN5A gene have been linked to Brugada syndrome (BrS), conduction disease, Long QT syndrome (LQT3), atrial fibrillation (AF), and to pre- and neonatal ventricular arrhythmias. OBJECTIVE The objective of this study is to characterize a novel mutation in Na(v)1.5 found in a newborn with fetal chaotic atrial tachycardia, post… (More)
DOI: 10.1139/y11-070

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