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Article

Molecular and clinical aspects of inherited cardiomyopathies.

Annals of medicine - 1 Jun 1995

Durand J B, Abchee A B, Roberts R

Abstract excerpt

Hypertrophic cardiomyopathy (HCM) is phenotypically and genotypically a heterogeneous disease. Since 1989, four chromosomal loci have been identified for HCM and the genes residing on three of these have been identified as beta-myosin heavy chain (beta-MHC), cardiac troponin-T and alpha-tropomyosin. These genes code for sarcomeric proteins and exhibit the same phenotype, suggesting that HCM is a disease of the...

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Source

Identifiers

PMID: 7546620
DOI: 10.3109/07853899509002583

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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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