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Article

The SCN5A mutation A1180V is associated with electrocardiographic features of LQT3.

Pediatric cardiology - 1 Feb 2014

Zhang Yanmin, Wang Juanli, Chang Suer, Zhou Nan, Xing Haijian, Wang Lei, Huang Chen, Ma Aiqun, Huang Christopher L-H, Lei Ming, Fraser James A

Abstract excerpt

Mutations of the SCN5A gene are associated with several arrhythmic syndromes including the Brugada syndrome, conduction disease, long QT syndrome type 3 (LQT3), atrial fibrillation, and dilated cardiomyopathy. We report LQT3 associated with an A1180V cardiac sodium channel mutation, previously associated with cardiac conduction block, and dilated cardiomyopathy in three generations of a Chinese family. Clinical,...

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Identifiers

PMID: 23963187
DOI: 10.1007/s00246-013-0773-6

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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