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

Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia.

International journal of cardiology - 15 Apr 2015

Xi Yanwei, Honeywell Christina, Zhang Dapeng, Schwartzentruber Jeremy, Beaulieu Chandree L, Tetreault Martine, Hartley Taila, Marton Jennifer, Vidal Silvia M, Majewski Jacek, Aravind L, Gollob Michael, Boycott Kym M, Gow Robert M

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 Child, Preschool
Share to DNA
Share to DNA Mutational Analysis

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heart Conduction System

Share to Mutation

Share to Pedigree

Share to Troponin I

Source

Open in PubMed Open full text

Identifiers

PMID: 25791106
DOI: 10.1016/j.ijcard.2015.03.130
PMCID: PMC5938092

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia.PMID 25791106Read ↗

Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys).Semantic proximity Read ↗

TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy.Semantic proximity Read ↗

Reduced kinase function in two ultra-rare TNNI3K variants in families with congenital junctional ectopic tachycardia.Semantic proximity Read ↗

Whole exome sequencing identifies a novel mutation (c.333 + 2T > C) of TNNI3K in a Chinese family with dilated cardiomyopathy and cardiac conduction disease.Semantic proximity Read ↗

Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease and dilated cardiomyopathySemantic proximity Read ↗

Identification of rare variants in TNNI3 with atrial fibrillation in a Chinese GeneID population.Semantic proximity Read ↗

Expanding the Recessive Spectrum of Dilated Cardiomyopathy: RNA-Level Validation of a Homozygous CTNNA3 Splice-Site Variant.Semantic proximity Read ↗

A rising titan: TTN review and mutation update.Semantic proximity Read ↗

Identification of <i>TTN</i> as a novel candidate gene for atrioventricular block in a Chinese pedigree by whole-exome sequencingSemantic proximity Read ↗

Analysis of TTN Truncating Variants in >74 000 Cases Reveals New Clinically Relevant Gene RegionsSemantic proximity Read ↗

New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia.Semantic proximity Read ↗

Single-Nucleotide Variations in Cardiac Arrhythmias: Prospects for Genomics and Proteomics Based Biomarker Discovery and DiagnosticsSemantic proximity Read ↗

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