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Article

Mapping a cardiomyopathy locus to chromosome 3p22-p25.

The Journal of clinical investigation - 15 Jan 1996

Olson T M, Keating M T

Abstract excerpt

Dilated cardiomyopathy (DCM) is a common disorder characterized by cardiac dilation and reduced systolic function. To identify a cardiomyopathy gene, we studied a family with DCM associated with sinus node dysfunction, supraventricular tachyarrhythmias, conduction delay, and stroke. A general lin...

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Share to Cardiomyopathy, Dilated
Share to Chromosomes, Human, Pair 3
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 8567977
DOI: 10.1172/JCI118445
PMCID: PMC507047

Genes

GNAI2
ITPR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-8567977-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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Mapping a cardiomyopathy locus to chromosome 3p22-p25.PMID 8567977Read ↗

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Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23.Semantic proximity Read ↗

Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.Semantic proximity Read ↗

Genome wide association analysis in dilated cardiomyopathy reveals two new key players in systolic heart failure on chromosome 3p25.1 and 22q11.23Semantic proximity Read ↗

Construction of a high-resolution physical map of the chromosome 10q22-q23 dilated cardiomyopathy locus and analysis of candidate genes.Semantic proximity Read ↗

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