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Article

Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy.

Circulation. Cardiovascular genetics - 1 Oct 2009

Kaski Juan Pablo, Syrris Petros, Esteban Maria Teresa Tome, Jenkins Sharon, Pantazis Antonios, Deanfield John E, McKenna William J, Elliott Perry M

Abstract excerpt

BACKGROUND: Hypertrophic cardiomyopathy (HCM) in infants and children is thought to be commonly associated with metabolic disorders and malformation syndromes. Familial disease caused by mutations in cardiac sarcomere protein genes, which accounts for most cases in adolescents and adults, is beli...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20031618
DOI: 10.1161/CIRCGENETICS.108.821314

Genes

MYBPC3
MYH7
MYL3
TNNI3
TNNT2
DES
MYL2
PRKAG2
TNNC1
TPM1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20031618-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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