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Article

Hypertrophic cardiomyopathy: a new mutation illustrates the need for family-centered care.

Pediatric cardiology - 1 Dec 2014

Lee Daniel D, Veith Regan L, Dimmock David P, Samyn Margaret M

Abstract excerpt

This is a case series of a family positive for a previously undescribed mutation in the myofilament gene MYH7, causing hypertrophic cardiomyopathy (HCM), a potentially lethal cardiac disease with strong hereditability. The family's significant disease became strikingly apparent with the unanticip...

Read the complete abstract on PubMed

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Share to Cardiac Myosins
Share to Cardiomyopathy, Hypertrophic, Familial
Share to Child, Preschool

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Infant, Newborn

Share to Myosin Heavy Chains

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Source

Identifiers

PMID: 25182012
DOI: 10.1007/s00246-014-1002-7

Genes

MYH7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-25182012-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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