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Article

Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy.

Circulation. Cardiovascular genetics - 1 Feb 2013

Wooten Eric C, Hebl Virginia B, Wolf Matthew J, Greytak Sarah R, Orr Nicole M, Draper Isabelle, Calvino Jenna E, Kapur Navin K, Maron Martin S, Kullo Iftikhar J, Ommen Steve R, Bos J Martijn, Ackerman Michael J, Huggins Gordon S

Abstract excerpt

BACKGROUND: Incomplete penetrance and variable expression of hypertrophic cardiomyopathy (HCM) is well appreciated. Common genetic polymorphisms variants that may affect HCM penetrance and expression have been predicted but are not well established. METHODS AND RESULTS: We performed a case-control genomewide association study to identify common HCM-associated genetic polymorphisms and then asked whether such...

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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: 23255317
DOI: 10.1161/CIRCGENETICS.112.965277
PMCID: PMC3578062

Genes

FHOD3

Variants

rs2303510

Provenance

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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