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

[Hypertrophic cardiomyopathy: infrequent mutation of the cardiac beta-myosin heavy-chain gene].

Revista espanola de cardiologia - 1 Aug 2006

Mora Roberto, Merino José L, Peinado Rafael, Olias Fernando, García-Guereta Luis, del Cerro María J, Tarín María N, Molano Jesús

Abstract excerpt

The aim of this study was to identify mutations in the cardiac heavy-chain beta-myosin gene (MYH7b) in a group of Spanish patients with hypertrophic cardiomyopathy. The study included 36 families with at least one member who had hypertrophic cardiomyopathy. DNA from exons 3 to 24 of the MYH7b gene was sequenced. Two mutations were identified: Arg858Cys and Met515Val. They occurred in two families, one of which...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Aged

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cardiac Myosins

Share to Cardiomyopathy, Hypertrophic

Share to Child, Preschool

Share to Myosin Heavy Chains

Share to Pedigree

Source

Identifiers

PMID: 16938236

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

[Hypertrophic cardiomyopathy: infrequent mutation of the cardiac beta-myosin heavy-chain gene].PMID 16938236Read ↗

Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

[Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

[Mutation analysis of beta myosin heavy chain gene in hypertrophic cardiomyopathy families].Semantic proximity Read ↗

Hypertrophic cardiomyopathy: low frequency of mutations in the beta-myosin heavy chain (MYH7) and cardiac troponin T (TNNT2) genes among Spanish patients.Semantic proximity Read ↗

Comprehensive analysis of the beta-myosin heavy chain gene in 389 unrelated patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

A novel mutation of the beta myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.Semantic proximity Read ↗

[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

Genetic variations of beta-MYH7 in Venezuelan patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

[Analysis of genotype and phenotype correlation of MYH7-V878A mutation among ethnic Han Chinese pedigrees affected with hypertrophic cardiomyopathy].Semantic proximity Read ↗

Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in Italian patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

[The role of mutation in cardiac beta-myosin heavy chain gene in population of patients].Semantic proximity Read ↗

[Study of mutations causing hypertrophic cardiomyopathy in a group of patients from Espirito Santo, Brazil].Semantic proximity Read ↗

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