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Article

LQTS gene LOVD database.

Human mutation - 1 Nov 2010

Zhang Tao, Moss Arthur, Cong Peikuan, Pan Min, Chang Bingxi, Zheng Liangrong, Fang Quan, Zareba Wojciech, Robinson Jennifer, Lin Changsong, Li Zhongxiang, Wei Junfang, Zeng Qiang, Qi Ming

Abstract excerpt

The Long QT Syndrome (LQTS) is a group of genetically heterogeneous disorders that predisposes young individuals to ventricular arrhythmias and sudden death. LQTS is mainly caused by mutations in genes encoding subunits of cardiac ion channels (KCNQ1, KCNH2,SCN5A, KCNE1, and KCNE2). Many other genes involved in LQTS have been described recently(KCNJ2, AKAP9, ANK2, CACNA1C, SCNA4B, SNTA1, and CAV3). We created an...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Open in PubMed Open full text

Identifiers

PMID: 20809527
DOI: 10.1002/humu.21341
PMCID: PMC3037562

Genes

KCNH2
AKAP9
ANK2
CAV3
KCNJ2
KCNQ1
SNTA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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