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Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome

15 Feb 2023

Abstract excerpt

BACKGROUND: A variant in the SLC4A3 anion exchanger has been identified as a novel cause of short QT syndrome (SQTS), but the clinical importance of SLC4A3 as a cause of SQTS or sudden cardiac death remains unknown. OBJECTIVE: The purpose of this study was to investigate the prevalence of potential disease-causing variants in SQTS patients using gene panels including SLC4A3. METHODS: In this multicenter study,...

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Share to Cardiac electrophysiology and arrhythmias
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PMID: 36806574
DOI: 10.1016/j.hrthm.2023.02.010

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