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Article

Histologic characterization of hypertrophic cardiomyopathy with and without myofilament mutations.

American heart journal - 1 Nov 2009

McLeod Christopher J, Bos J Martijn, Theis Jeanne L, Edwards William D, Gersh Bernard J, Ommen Steve R, Ackerman Michael J

Abstract excerpt

BACKGROUND: Between 30% and 60% of clinical cases of hypertrophic cardiomyopathy (HC) can be attributed to mutations in the genes encoding cardiac myofilament proteins. Interestingly, it appears that the likelihood of an underlying myofilament mutation can be predicted by echocardiographic assess...

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Identifiers

PMID: 19853701
DOI: 10.1016/j.ahj.2009.09.006
PMCID: PMC3281581

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19853701-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

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

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