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Article

Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome.

American journal of medical genetics - 2 Oct 1996

Satler C A, Walsh E P, Vesely M R, Plummer M H, Ginsburg G S, Jacob H J

Abstract excerpt

Autosomal-dominant long QT syndrome (LQT) is an inherited disorder, predisposing affected individuals to sudden death from tachyarrhythmias. To identify the gene(s) responsible for LQT, we identified and characterized an LQT family consisting of 48 individuals. DNA was screened with 150 microsate...

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Identifiers

PMID: 8914737
DOI: 10.1002/(SICI)1096-8628(19961002)65:1<27::AID-AJMG4>3.0.CO;2-V

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-8914737-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome.PMID 8914737Read ↗

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A mutation in HERG associated with notched T waves in long QT syndrome.Semantic proximity Read ↗

Molecular genetics of long QT syndrome.Semantic proximity Read ↗

A novel splice mutation of HERG in a Chinese family with long QT syndrome.Semantic proximity Read ↗

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