Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

American journal of human genetics - 1 Oct 1999

Jung M, Poepping I, Perrot A, Ellmer A E, Wienker T F, Dietz R, Reis A, Osterziel K J

Abstract excerpt

Dilated cardiomyopathy (DCM) is a leading cause of heart failure and the most frequent indication for heart transplantation in young patients. Probably >25% of DCM cases are of familial etiology. We report here genetic localization in a three-generation German family with 12 affected individuals with autosomal dominant familial DCM characterized by ventricular dilatation, impaired systolic function, and...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cardiomyopathy, Dilated
Share to Chromosome Mapping

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 2

Share to Genes, Dominant

Share to Genetic Heterogeneity

Share to Germany

Share to Lod Score

Share to Pedigree

Source

Open in PubMed Open full text

Identifiers

PMID: 10486326
DOI: 10.1086/302580
PMCID: PMC1288240

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22.PMID 10486326Read ↗

A novel locus for autosomal-dominant dilated cardiomyopathy maps to chromosome 7q22.3-31.1.Semantic proximity Read ↗

Familial Dilated Cardiomyopathy Locus Maps to Chromosome 2q31Semantic 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 ↗

Mapping a cardiomyopathy locus to chromosome 3p22-p25.Semantic proximity Read ↗

A novel locus for dilated cardiomyopathy maps to canine chromosome 8.Semantic proximity Read ↗

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

A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26.Semantic proximity Read ↗

The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23–q24Semantic proximity Read ↗

A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.Semantic proximity Read ↗

A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.Semantic proximity Read ↗

A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.