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Article

New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.

Circulation - 7 Apr 1998

Li H, Chen Q, Moss A J, Robinson J, Goytia V, Perry J C, Vincent G M, Priori S G, Lehmann M H, Denfield S W, Duff D, Kaine S, Shimizu W, Schwartz P J, Wang Q, Towbin J A

Abstract excerpt

BACKGROUND: Long-QT syndrome (LQTS) is an inherited cardiac arrhythmia that causes sudden death in young, otherwise healthy people. Four genes for LQTS have been mapped to chromosome 11p15.5 (LQT1), 7q35-36 (LQT2), 3p21-24 (LQT3), and 4q25-27 (LQT4). Genes responsible for LQT1, LQT2, and LQT3 have been identified as cardiac potassium channel genes (KVLQT1, HERG) and the cardiac sodium channel gene (SCN5A)....

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Identifiers

PMID: 9570196
DOI: 10.1161/01.cir.97.13.1264

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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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