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Article

Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy.

BMC medical genetics - 30 Apr 2010

Rodríguez-García María Isabel, Monserrat Lorenzo, Ortiz Martín, Fernández Xusto, Cazón Laura, Núñez Lucía, Barriales-Villa Roberto, Maneiro Emilia, Veira Elena, Castro-Beiras Alfonso, Hermida-Prieto Manuel

Abstract excerpt

BACKGROUND: MyBPC3 mutations are amongst the most frequent causes of hypertrophic cardiomyopathy, however, its prevalence varies between populations. They have been associated with mild and late onset disease expression. Our objectives were to establish the prevalence of MyBPC3 mutations and dete...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 20433692
DOI: 10.1186/1471-2350-11-67
PMCID: PMC2880974

Genes

MYH7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20433692-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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