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Article

A double heterozygous variant in MYH6 and MYH7 associated with hypertrophic cardiomyopathy in a Japanese Family

22 Oct 2021

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 35911064
DOI: 10.1016/j.jccase.2021.09.011

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A double heterozygous variant in MYH6 and MYH7 associated with hypertrophic cardiomyopathy in a Japanese FamilyPMID 35911064Read ↗

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

MYH7 Rare Variant in a Family With Double-Chambered Left Ventricle.Semantic proximity Read ↗

A novel MYH7 mutation in a family with cardiomyopathy presenting with restrictive physiology and varying degrees of left ventricle hypertrophy.Semantic proximity Read ↗

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

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

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

Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy.Semantic proximity Read ↗

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

One third of Danish hypertrophic cardiomyopathy patients have mutations in MYH7 rod regionSemantic proximity Read ↗

Carrying both the heterozygous Myh6-R453C and Tnnt2-R92W mutations aggravate the hypertrophic cardiomyopathy phenotype in mice.Semantic proximity Read ↗

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

Genetic screening and double mutation in Japanese patients with hypertrophic cardiomyopathy.Semantic proximity Read ↗

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