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Article

One third of Danish hypertrophic cardiomyopathy patients have mutations in MYH7 rod region

13 Oct 2004

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 15483641
DOI: 10.1038/sj.ejhg.5201310

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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.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

One third of Danish hypertrophic cardiomyopathy patients have mutations in MYH7 rod regionPMID 15483641Read ↗

A double heterozygous variant in MYH6 and MYH7 associated with hypertrophic cardiomyopathy in a Japanese FamilySemantic proximity Read ↗

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

Novel Mutations in β-MYH7 Gene in Indian Patients With Dilated CardiomyopathySemantic proximity Read ↗

Coexistence of Digenic Mutations in Both Thin (TPM1) and Thick (MYH7) Filaments of Sarcomeric Genes Leads to Severe Hypertrophic Cardiomyopathy in a South Indian FHCM.Semantic proximity Read ↗

Founder mutations in hypertrophic cardiomyopathy patients in the NetherlandsSemantic proximity Read ↗

Homozygous mutation in MYH7 in myosin storage myopathy and cardiomyopathy.Semantic proximity Read ↗

Hypertrophic cardiomyopathy: from mutation to functional analysis of defective protein.Semantic proximity Read ↗

MYH7-related disorders in two Bulgarian families: Novel variants in the same region associated with different clinical manifestation and disease penetrance.Semantic proximity Read ↗

Novel mutation in MYH7 gene associated with distal myopathy and cardiomyopathy.Semantic proximity Read ↗

[Familial hypertrophic cardiomyopathy--a case report].Semantic proximity Read ↗

Novel Missense Variant in MYL2 Gene Associated With Hypertrophic Cardiomyopathy Showing High Incidence of Restrictive PhysiologySemantic proximity Read ↗

New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7.Semantic proximity Read ↗

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