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

Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.

Circulation. Cardiovascular genetics - 1 Oct 2009

Dellefave Lisa M, Pytel Peter, Mewborn Stephanie, Mora Bassem, Guris Deborah L, Fedson Savitri, Waggoner Darrel, Moskowitz Ivan, McNally Elizabeth M

Abstract excerpt

BACKGROUND: Mutations in the genes encoding sarcomere proteins have been associated with both hypertrophic and dilated cardiomyopathy. Recently, mutations in myosin heavy chain (MYH7), cardiac actin (ACTC), and troponin T (TNNT2) were associated with left ventricular noncompaction, a form of card...

Read the complete abstract on PubMed

Topics

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

Share to Cardiac Myosins
Share to Carrier Proteins
Share to Hypertrophy, Left Ventricular

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant

Share to Infant, Newborn

Share to Myosin Heavy Chains

Share to Sarcomeres

Share to Ultrasonography

Source

Identifiers

PMID: 20031619
DOI: 10.1161/CIRCGENETICS.109.861955

Genes

MYH7
MYBPC3
TNNT2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20031619-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Sarcomere mutations in cardiomyopathy with left ventricular hypertrabeculation.PMID 20031619Read ↗

Mutations in sarcomere protein genes in left ventricular noncompaction.Semantic proximity Read ↗

Sarcomere mutations in cardiogenesis and ventricular noncompaction.Semantic proximity Read ↗

Sarcomere gene variants act as a genetic trigger underlying the development of left ventricular noncompaction.Semantic proximity Read ↗

Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype.Semantic proximity Read ↗

Clinical features and outcome of hypertrophic cardiomyopathy associated with triple sarcomere protein gene mutations.Semantic proximity Read ↗

Case Report of Left Ventricular Noncompaction Cardiomyopathy Characterized by Undulating Phenotypes in Adult Patients.Semantic proximity Read ↗

Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy.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 ↗

Mutations in Sarcomere Protein Genes as a Cause of Dilated CardiomyopathySemantic proximity Read ↗

[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy].Semantic proximity Read ↗

A novel cardiac myosin-binding protein C S297X mutation in hypertrophic cardiomyopathy.Semantic proximity Read ↗

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