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Article

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

International journal of cardiology - 15 May 2014

Finsterer Josef, Stöllberger Claudia, Brandau Oliver, Laccone Franco, Bichler Katharina, Laing Nigel G

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Topics

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Share to Arrhythmias, Cardiac
Share to Cardiac Myosins
Share to MYH7 gene
Share to Heart Defects, Congenital

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

Share to Muscular Diseases

Share to Mutation

Share to Myosin Heavy Chains

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Source

Identifiers

PMID: 24726209
DOI: 10.1016/j.ijcard.2014.03.025

Genes

MYH7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

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

Research trail→

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Novel MYH7 mutation associated with mild myopathy but life-threatening ventricular arrhythmias and noncompaction.PMID 24726209Read ↗

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

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A Wide and Specific Spectrum of Genetic Variants and Genotype-Phenotype Correlations Revealed by Next-Generation Sequencing in Patients with Left Ventricular Noncompaction.Semantic proximity Read ↗

[Clinical phenotype and genetic analysis of patients with left ventricular noncompaction caused by the biallelic mutation of MYBPC3 and 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 ↗

Genetic Analysis of Patients with Left Ventricular Noncompaction: Identification of Novel Candidate VariantsSemantic proximity Read ↗

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

A Splice Variant of the MYH7 Gene Is Causative in a Family with Isolated Left Ventricular Noncompaction Cardiomyopathy.Semantic proximity Read ↗

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

MYH7 in cardiomyopathy and skeletal muscle myopathy.Semantic proximity Read ↗

Distal myosin heavy chain-7 myopathy due to the novel transition c.5566G>A (p.E1856K) with high interfamilial cardiac variability and putative anticipation.Semantic proximity Read ↗

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