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Article

Molecular genetic studies of familial hypertrophic cardiomyopathy.

Basic research in cardiology - 1 Jan 1998

Seidman C E, Seidman J G

Abstract excerpt

Molecular genetic studies of FHC have defined this as disease of the sarcomere. Multiple different mutations in six disease genes, which appear to act through a dominant negative mechanism, have been identified. A relevant murine model of human FHC has been developed. Assessment of the influences...

Topics

Animals
Cardiomyopathy, Hypertrophic
Humans
Mutation
Troponin T

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9879437
DOI: 10.1007/s003950050196

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9879437-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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