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Article

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

European heart journal - 14 Jan 2015

Yu Bi-lian, Xiang Rong, Hu Die, Peng Dao-quan

Abstract excerpt

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Topics

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Share to Cardiac Myosins
Share to Cardiomyopathy, Hypertrophic, Familial
Share to Cardiomyopathy, Restrictive
Share to Child

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

Share to Hypertrophy, Left Ventricular

Share to Myosin Heavy Chains

Share to Pedigree

Share to Young Adult

Source

Identifiers

PMID: 25422285
DOI: 10.1093/eurheartj/ehu435

Genes

MYH7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 21 Oct 2026.

Related research

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

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel MYH7 mutation in a family with cardiomyopathy presenting with restrictive physiology and varying degrees of left ventricle hypertrophy.PMID 25422285Read ↗

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

Restrictive Physiology Associated with an MYH7 Mutation in the Absence of Hypertrophy: A Multimodality Imaging Case ReportSemantic proximity Read ↗

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

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

Novel MYH7 mutation associated with mild myopathy but life-threatening ventricular arrhythmias and noncompaction.Semantic proximity Read ↗

MYH7 variants cause complex congenital heart disease.Semantic proximity Read ↗

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

[Phenotype and genotype characteristics of children with cardiomyopathy associated with MYH7 gene mutation: a retrospective analysis].Semantic proximity Read ↗

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

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

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

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