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


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


Figures and Tables

Sorry, we couldn't extract any figures or tables for this paper.

Slides referencing similar topics