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

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

The Journal of thoracic and cardiovascular surgery - 1 Nov 2014

Hirono Keiichi, Hata Yukiko, Ibuki Keijirou, Yoshimura Naoki

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 Abnormalities, Multiple
Share to Cardiac Myosins
Share to Heart Defects, Congenital
Share to Heart Septal Defects, Ventricular

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heredity

Share to Infant, Newborn

Share to Mutation, Missense

Share to Myosin Heavy Chains

Source

Identifiers

PMID: 25444217
DOI: 10.1016/j.jtcvs.2014.08.049

Genes

MYH7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial Ebstein's anomaly, left ventricular noncompaction, and ventricular septal defect associated with an MYH7 mutation.PMID 25444217Read ↗

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

Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7.Semantic proximity Read ↗

Mutations in the sarcomere gene MYH7 in Ebstein anomaly.Semantic proximity Read ↗

Ebstein's anomaly.Semantic proximity Read ↗

Ebstein’s anomaly may be caused by mutations in the sarcomere protein gene MYH7Semantic proximity Read ↗

Ebstein's Anomaly: Genetics, Clinical Manifestations, and Management.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 variants cause complex congenital heart disease.Semantic proximity Read ↗

Surgical repair of left ventricular noncompaction in a patient with a novel mutation of the myosin heavy chain 7 gene.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 ↗

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

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