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Article

[Mutations genes in primarly cardiomyopathies].

Medicinski arhiv - 1 Jan 2007

Baraković Fahir, Kusljugić Zumreta, Masić Izet

Abstract excerpt

Diagnosis of primarly cardiomypathies refers to genes discorders in chromosomes. Aim of this paper is to show genetics and molecular knowledges published so far. Familiar form hypertrophic cardiomyopathy is hereditable autosomatically dominantly in any of 10 genes that regulate contractile, structural and regulative function with predomination of mutation in gene for heavy chaire of myocardiac beta myosin...

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Share to Arrhythmogenic Right Ventricular Dysplasia
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Share to Cardiomyopathy, Dilated

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Source

Identifiers

PMID: 21553441

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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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