Familial hypertrophic cardiomiopathy: molecular basis and genotype-phenotype correlations.

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Article

Familial hypertrophic cardiomiopathy: molecular basis and genotype-phenotype correlations.

Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology - 1 Oct 1998

Cuda G, Lamberti A, Perrotti N, Perticone F, Mattioli P L

Abstract excerpt

The impact of molecular genetics in the diagnosis and management of various forms of heritable cardiac or vascular disorders is continuously increasing thanks to the newly available laboratory tools. Familial hypertrophic cardiomyopathy (FHC), an autosomal dominant inherited disease characterized...

Topics

Animals
Cardiomyopathy, Hypertrophic
Chickens
Genotype
Humans
Myosin Heavy Chains
Myosin Light Chains
Phenotype
Protein C
Troponin T

Source

Open in PubMed

Identifiers

PMID: 9835779

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9835779-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

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

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