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Article

Genetic basis of hypertrophic cardiomyopathy.

Expert review of cardiovascular therapy - 1 Nov 2006

Lind Joanne M, Chiu Christine, Semsarian Christopher

Abstract excerpt

Hypertrophic cardiomyopathy (HCM) was the first cardiovascular disorder in which a genetic basis was identified. The disease is characterized by a marked thickening of the left ventricle and is the most common structural cause of sudden cardiac death in those aged under 35 years. HCM is primarily a disease of the sarcomere with over 250 mutations identified currently within 13 sarcomere-related genes. At present,...

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Identifiers

PMID: 17173506
DOI: 10.1586/14779072.4.6.927

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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