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

CALM3 mutation associated with long QT syndrome.

Heart rhythm - 1 Feb 2015

Reed Griffin J, Boczek Nicole J, Etheridge Susan P, Ackerman Michael J

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 Cardiac electrophysiology and arrhythmias
Share to DNA
Share to DNA Mutational Analysis
Share to Electrocardiography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Long QT Syndrome

Share to Monomeric Clathrin Assembly Proteins

Share to Mutation

Share to Pedigree

Source

Open in PubMed Open full text

Identifiers

PMID: 25460178
DOI: 10.1016/j.hrthm.2014.10.035
PMCID: PMC4907373

Genes

CALM3

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

CALM3 mutation associated with long QT syndrome.PMID 25460178Read ↗

Calmodulin mutations can underlie the phenotype of long QT syndrome variant 1.Semantic proximity Read ↗

Molecular genetics of inherited long QT syndromes.Semantic proximity Read ↗

Molecular basis of congenital and acquired long QT syndromes.Semantic proximity Read ↗

Case report of a child with long QT syndrome type 14 caused by CALM1 gene mutation and literature review.Semantic proximity Read ↗

Molecular genetics of long QT syndromeSemantic proximity Read ↗

Calmodulin Mutations Associated with Heart Arrhythmia: A Status ReportSemantic proximity Read ↗

Spectrum and Prevalence of <i>CALM1</i> -, <i>CALM2</i> -, and <i>CALM3</i> -Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome–Associated Calmodulin Missense Variant, E141GSemantic proximity Read ↗

Novel calmodulin mutations associated with congenital arrhythmia susceptibility.Semantic proximity Read ↗

Calmodulin Mutations in Human Disease.Semantic proximity Read ↗

Genetic Mosaicism in CalmodulinopathySemantic proximity Read ↗

Molecular basis of the long-QT syndrome associated with deafness.Semantic proximity Read ↗

Generation of a human induced pluripotent stem cell line ZZUNEUi030-A from a female patient carrying a heterozygous CALM2 (c.395 A > T) mutation.Semantic proximity Read ↗

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