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

[Molecular basis of heart failure and dilated cardiomyopathy].

Herz - 1 Dec 2002

Osterziel Karl Josef, Perrot Andreas

Abstract excerpt

Dilated cardiomyopathy (DCM) is one of the leading causes of heart failure. Several prospective studies have shown that about 25-30% of all cases are of familial etiology. The most common mode of inheritance is autosomal dominant. Less frequently is inheritance as an X-chromosomal trait. Examination of families has identified nine disease genes so far. The penetrance of the identified mutations is highly variable...

Read the complete abstract on PubMed

Topics

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

Share to Acyltransferases
Share to Cardiomyopathy, Dilated
Share to Chromosomes, Human, X

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Dystrophin

Share to Heart Failure

Share to Sarcomeres

Share to Sex Chromosome Aberrations

Share to Ventricular Dysfunction, Left

Source

Identifiers

PMID: 12596715

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Molecular basis of heart failure and dilated cardiomyopathy].PMID 12596715Read ↗

[Genetics of dilated cardiomyopathy].Semantic proximity Read ↗

Genetics and Molecular Mechanisms of Idiopathic Dilated Cardiomyopathy, a Possible Guide to Individualized ManagementSemantic proximity Read ↗

Comprehensive review on gene mutations contributing to dilated cardiomyopathySemantic proximity Read ↗

Dilated cardiomyopathy: a new insight into the rare but common cause of heart failure.Semantic proximity Read ↗

Pathophysiology of dilated cardiomyopathy: from mechanisms to precision medicine.Semantic proximity Read ↗

[Review: genetics of familial dilated cardiomyopathy].Semantic proximity Read ↗

Genetic mutations and mechanisms in dilated cardiomyopathy.Semantic proximity Read ↗

Hereditary dilated cardiomyopathy.Semantic proximity Read ↗

Dilated Cardiomyopathy: A New Era of TreatmentSemantic proximity Read ↗

[Familial dilated cardiomyopathy].Semantic proximity Read ↗

Genetic abnormalities responsible for dilated cardiomyopathy.Semantic proximity Read ↗

Genetics of Dilated Cardiomyopathy.Semantic proximity Read ↗

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