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Article

Beta-myosin heavy chain gene mutations and hypertrophic cardiomyopathy in Austrian children.

Journal of molecular and cellular cardiology - 1 Jan 2001

Greber-Platzer S, Marx M, Fleischmann C, Suppan C, Dobner M, Wimmer M

Abstract excerpt

Hypertrophic cardiomyopathy occurs in two variants, either as an autosomal dominant familial disorder or as a sporadic disease without familial involvement. Different genes coding sarcomeric proteins of the heart have been identified as causing hypertrophic cardiomyopathy. Missense mutations in the cardiac beta-myosin heavy chain gene are found in 30% of all cases of familial hypertrophic cardiomyopathy. We...

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Identifiers

PMID: 11133230
DOI: 10.1006/jmcc.2000.1287

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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.

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