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

Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.

International journal of medical sciences - 1 Jan 2014

Yu Hong, Xu Jia-Hong, Song Hao-Ming, Zhao Lan, Xu Wen-Jun, Wang Juan, Li Ruo-Gu, Xu Lei, Jiang Wei-Feng, Qiu Xing-Biao, Jiang Jin-Qi, Qu Xin-Kai, Liu Xu, Fang Wei-Yi, Jiang Jin-Fa, Yang Yi-Qing

Abstract excerpt

Atrial fibrillation (AF) is the most common form of sustained cardiac arrhythmia in humans and is responsible for substantial morbidity and mortality worldwide. Emerging evidence indicates that abnormal cardiovascular development is involved in the pathogenesis of AF. In this study, the coding exons and splice sites of the NKX2-5 gene, which encodes a homeodomain-containing transcription factor essential for...

Read the complete abstract on PubMed

Topics

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

Share to Asian People
Share to Atrial Fibrillation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homeobox Protein Nkx-2.5

Share to Homeodomain Proteins

Share to Precision Medicine

Share to RNA Splice Sites

Share to Sequence Alignment

Share to Structure-Activity Relationship

Source

Open in PubMed Open full text

Identifiers

PMID: 24782644
DOI: 10.7150/ijms.8407
PMCID: PMC4003540

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.PMID 24782644Read ↗

A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.Semantic proximity Read ↗

Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation.Semantic proximity Read ↗

Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation.Semantic proximity Read ↗

A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmiasSemantic proximity Read ↗

A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation.Semantic proximity Read ↗

Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block.Semantic proximity Read ↗

NKX2-6 mutation predisposes to familial atrial fibrillation.Semantic proximity Read ↗

TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome.Semantic proximity Read ↗

Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation.Semantic proximity Read ↗

A novel PITX2c loss‑of‑function mutation underlies lone atrial fibrillation.Semantic proximity Read ↗

A novel NKX2.5 loss-of-function mutation associated with congenital bicuspid aortic valve.Semantic proximity Read ↗

Novel NKX2-5 mutations in patients with familial atrial septal defects.Semantic proximity Read ↗

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