Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

MYH7 Rare Variant in a Family With Double-Chambered Left Ventricle.

Circulation. Cardiovascular genetics - 1 Dec 2017

Wang Jing, Zhang Xin, Wang Xi, Wang Chuchu, Wang Fangyun, Wang Binbin

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amino Acid Substitution
Share to Cardiac Myosins
Share to Child, Preschool
Share to Heart Ventricles

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

Share to Heterozygote

Share to Mutation, Missense

Share to Myosin Heavy Chains

Share to Pedigree

Source

Identifiers

PMID: 29237678
DOI: 10.1161/CIRCGENETICS.117.001729

Genes

MYH7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

MYH7 Rare Variant in a Family With Double-Chambered Left Ventricle.PMID 29237678Read ↗

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

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

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 ↗

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

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

Diverse cardiac phenotypes among different carriers of the same MYH7 splicing variant allele (c.732+1G>A) from a family.Semantic proximity Read ↗

Clinical Features and Outcomes of Pediatric MYH7-Related Dilated Cardiomyopathy.Semantic proximity Read ↗

Familial Ebstein's anomaly, left ventricular noncompaction, and ventricular septal defect associated with an MYH7 mutation.Semantic proximity Read ↗

Familial ebstein anomaly, left ventricular hypertrabeculation, and ventricular septal defect associated with a MYH7 mutation.Semantic proximity Read ↗

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

Description of a novel mutation leading to MYH9-related disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.