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Article

ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome.

Circulation - 15 Nov 1995

Moss A J, Zareba W, Benhorin J, Locati E H, Hall W J, Robinson J L, Schwartz P J, Towbin J A, Vincent G M, Lehmann M H

Abstract excerpt

BACKGROUND: The long QT syndrome is an inherited disorder with prolonged ventricular repolarization and a propensity to ventricular tachyarrhythmias and sudden arrhythmic death. Recent linkage studies have demonstrated three separate loci for this disorder on chromosomes 3, 7, and 11, and specific mutated genes for long QT syndrome have been identified on two of these chromosomes. We investigated ECG T-wave...

Topics

Adult
Chromosome Mapping
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 7
Electrocardiography
Female
Genetic Linkage
Genotype
Heart
Humans

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Ion Channels

Long QT Syndrome

Male

Mutation

Phenotype

Source

Identifiers

PMID: 7586261
DOI: 10.1161/01.cir.92.10.2929

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 29 Aug 2026. Prepared record publication-7586261-2026-08-29.1. Manifest publication-graph-cohort-2026-08-29.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 29 Aug 2026.

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