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

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

Clinical cardiology - 1 Sept 2009

Wang Juan, Xu Shi-Jie, Zhou Hua, Wang Li-Jie, Hu Bo, Fang Fang, Zhang Xu-Min, Luo Yi-Wei, He Xiao-Yan, Zhuang Shao-Wei, Li Xin-Ming, Liu Zhong-Ming, Hu Da-Yi

Abstract excerpt

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disorder and shows high variability in genetic heterogeneity and phenotypic characteristics. The genetic etiology responsible for HCM in many individuals remains unclear. OBJECTIVE: This instigation was sought to identify novel genetic determinants for familial hypertrophic cardiomyopathy. METHODS: Six unrelated Chinese families...

Read the complete abstract on PubMed

Topics

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

Share to Cardiac Myosins
Share to Cardiomyopathy, Hypertrophic, Familial

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Echocardiography, Doppler

Share to Electrocardiography

Share to Microsatellite Repeats

Share to Mutation, Missense

Share to Myosin Heavy Chains

Share to Severity of Illness Index

Source

Open in PubMed Open full text

Identifiers

PMID: 19645038
DOI: 10.1002/clc.20520
PMCID: PMC6652898

Genes

MYH7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel mutation of the beta myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.PMID 19645038Read ↗

Asn391Thr Mutation of β-Myosin Heavy Chain in a Hypertrophic Cardiomyopathy Family.Semantic proximity Read ↗

Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy.Semantic proximity Read ↗

A MYH7 variant in a five-generation-family with hypertrophic cardiomyopathySemantic proximity Read ↗

[Analysis of phenotype and MYH7 gene variant in a family of patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

Variation p.R1045H in MYH7 correlated with hypertrophic cardiomyopathy in a Chinese pedigree.Semantic proximity Read ↗

Molecular Genetic Basis of Hypertrophic Cardiomyopathy.Semantic proximity Read ↗

Exome sequencing identifies a novel MYH7 p.G407C mutation responsible for familial hypertrophic cardiomyopathy.Semantic proximity Read ↗

Screening of MYH7 gene mutation sites in hypertrophic cardiomyopathy and its significance.Semantic proximity Read ↗

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

Variation p.R1045H in MYH7 correlated with hypertrophic cardiomyopathy in a Chinese pedigreeSemantic proximity Read ↗

Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated CardiomyopathySemantic proximity Read ↗

[Mutation and clinical relevance in a large cohort of unrelated Chinese patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

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