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Article

Mapping of a gene for long QT syndrome to chromosome 4q25-27.

American journal of human genetics - 1 Nov 1995

Schott J J, Charpentier F, Peltier S, Foley P, Drouin E, Bouhour J B, Donnelly P, Vergnaud G, Bachner L, Moisan J P

Abstract excerpt

Long QT syndrome (LQTS) is a heterogeneous inherited disorder causing syncope and sudden death from ventricular arrhythmias. A first locus for this disorder was mapped to chromosome 11p15.5. However, locus heterogeneity has been demonstrated in several families, and two other loci have recently been located on chromosomes 7q35-36 and 3p21-24. We used linkage analysis to map the locus in a 65-member family in...

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Identifiers

PMID: 7485162
PMCID: PMC1801360

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

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