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Article

[Familial hypertrophic cardiomyopathy--a case report].

Kardiologia polska - 1 Nov 2006

Domal-Kwiatkowska Dorota, Glanowska Grazyna, Smolik Sławomir, Wilczewski Przemysław, Mazurek Urszula, Nowalany-Kozielska Ewa, Fudal Marcin, Wodniecki Jan

Abstract excerpt

Genetic profile od four-generation family with hypertrophic cardiomyopathy is presented. The alterations in the MYH7 gene sequences were identified. Genetic background of familial hypertrophic cardiomyopathy is reviewed and discussed.

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Source

Identifiers

PMID: 17165166

Genes

MYH7

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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[Familial hypertrophic cardiomyopathy--a case report].PMID 17165166Read ↗

[Hypertrophic cardiomyopathy: New pathogenic variant in MYH7].Semantic proximity Read ↗

[Analysis of phenotype and MYH7 gene variant in a family of patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

A MYH7 variant in a five-generation-family with hypertrophic cardiomyopathySemantic proximity Read ↗

[Clinical and molecular genetics of hypertrophic cardiomyopathy].Semantic proximity Read ↗

[Recent research on childhood hypertrophic cardiomyopathy caused by MYH7 gene mutations].Semantic proximity Read ↗

[Analysis of genotype and phenotype correlation of MYH7-V878A mutation among ethnic Han Chinese pedigrees affected with hypertrophic cardiomyopathy].Semantic proximity Read ↗

Variation p.R1045H in MYH7 correlated with hypertrophic cardiomyopathy in a Chinese pedigreeSemantic proximity Read ↗

[Familial hypertrophic cardiomyopathy: genes, mutations and animal models. A review].Semantic proximity Read ↗

A novel mutation of the beta myosin heavy chain gene responsible for familial hypertrophic cardiomyopathy.Semantic proximity Read ↗

[Correlation between genotype and clinical phenotype in hypertrophic cardiomyopathy families with MYH7-R453C mutation].Semantic proximity Read ↗

[Profiles of genotypes of familial hypertrophic cardiomyopathy according to data of clinical studies].Semantic proximity Read ↗

[Genotype-phenotype correlations in familial hypertrophic cardiomyopathy].Semantic proximity Read ↗

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