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Article

A malignant phenotype of hypertrophic cardiomyopathy caused by Arg719Gln cardiac beta-myosin heavy-chain mutation in a Chinese family.

Clinica chimica acta; international journal of clinical chemistry - 20 Aug 2001

Huang X, Song L, Ma A Q, Gao J, Zheng W, Zhou X, Zhang Q, Lu H, Li Y, Liu Y, Hui R

Abstract excerpt

Mutations of the cardiac beta-myosin heavy-chain (beta-MHC) gene cause hypertrophic cardiomyopathy (HCM). Recent genotype-phenotype correlation studies have shown that mutations carry prognostic significance. We studied five unrelated Chinese families with hypertrophic cardiomyopathy. Exons 3-27 and 40 of the beta-MHC gene were screened with both the polymerase chain reaction-single-strand conformation...

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Share to Cardiomyopathy, Hypertrophic

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

Share to Mutation, Missense

Share to Myosin Heavy Chains

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Share to Polymorphism, Single-Stranded Conformational

Source

Identifiers

PMID: 11498078
DOI: 10.1016/s0009-8981(01)00538-1

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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.

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