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

Familial hypertrophic cardiomyopathy. Insertion-deletion polymorphism of angiotensin-converting enzyme and angiotensin II receptor.

Kardiologia polska - 1 May 2005

Gilanowska Grazyna, Domal-Kwiatkowska Dorota, Smolik Sławomir, Wilczewski Przemysław, Szarek Jarosław, Nowalany-Kozielska Ewa, Mazurek Urszula, Wodniecki Jan, Wilczok Tadeusz

Abstract excerpt

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is a genetic-based disease. Several gene mutations leading to HCM development have been described. AIM: Detailed examination of phenotype and genotype of a family with HCM. METHODS: Clinical and genetic examinations were performed in a family with HCM, in which 3 sick persons with different disease phenotype were found. RESULTS: In all sick persons the same molecular...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Cardiomyopathy, Hypertrophic, Familial

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Deletion

Share to Pedigree

Share to Peptidyl-Dipeptidase A

Share to Polymorphism, Genetic

Share to Receptor, Angiotensin, Type 1

Share to Receptors, Angiotensin

Source

Identifiers

PMID: 15928721

Genes

ACE

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

Familial hypertrophic cardiomyopathy. Insertion-deletion polymorphism of angiotensin-converting enzyme and angiotensin II receptor.PMID 15928721Read ↗

Genetic polymorphism of angiotensin-converting enzyme and hypertrophic cardiomyopathy risk: A systematic review and meta-analysis.Semantic proximity Read ↗

Impact of polymorphisms in the renin-angiotensin-aldosterone system on hypertrophic cardiomyopathy.Semantic proximity Read ↗

The influence of Angiotensin converting enzyme and angiotensinogen gene polymorphisms on hypertrophic cardiomyopathy.Semantic proximity Read ↗

[Analysis of morpho-functional parameters of the heart and polymorphisms of Renin-Angiotensin-aldosterone system genes in patients with different variants of the course of hypertrophic cardiomyopathy].Semantic proximity Read ↗

Impact of angiotensin I converting enzyme insertion/deletion polymorphisms on dilated cardiomyopathy and hypertrophic cardiomyopathy risk.Semantic proximity Read ↗

Sudden cardiac death in patients with hypertrophic cardiomyopathy: from bench to bedside with an emphasis on genetic markers.Semantic proximity Read ↗

Genotype phenotype correlations of cardiac beta-myosin heavy chain mutations in Indian patients with hypertrophic and dilated cardiomyopathy.Semantic proximity Read ↗

Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac death.Semantic proximity Read ↗

Angiotensinogen M235T polymorphism and susceptibility to hypertrophic cardiomyopathy in Asian population: A meta analysis.Semantic proximity Read ↗

The M235T polymorphism of the angiotensinogen gene in South Indian patients of hypertrophic cardiomyopathy.Semantic proximity Read ↗

Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier.Semantic proximity Read ↗

[The effect of polymorphisms of the angiotensin-converting enzyme and angiotensinogen genes on the phenotypic expression of Spanish patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

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