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

[Novel NKX2-5 mutations identified in patients with congenital ventricular septal defects].

Zhonghua yi xue za zhi - 15 Sept 2009

Liu Xing-yuan, Yang Yi-qing, Yang Ying, Lin Xiao-ping, Chen Yi-han

Abstract excerpt

OBJECTIVE: To identify the novel genetic defects in patients with congenital ventricular septal defect (VSD). METHODS: The clinical data and blood samples from 160 unrelated subjects with congenital VSD were collected and evaluated in comparison with 200 healthy individuals. The coding exons and...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Case-Control Studies
Share to Heart Septal Defects, Ventricular

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homeobox Protein Nkx-2.5

Share to Homeodomain Proteins

Share to Regulatory Elements, Transcriptional

Share to Sequence Alignment

Share to Transcription Factors

Source

Identifiers

PMID: 20137692

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20137692-2026-09-02.2. 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

[Novel NKX2-5 mutations identified in patients with congenital ventricular septal defects].PMID 20137692Read ↗

[Mutation of NKX2-5 gene in patients with atrial septal defect].Semantic proximity Read ↗

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

Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population.Semantic proximity Read ↗

NKX2-5 variants screening in patients with atrial septal defect in IndonesiaSemantic proximity Read ↗

A novel NKX2-5 mutation in familial ventricular septal defectSemantic proximity Read ↗

Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a Novel NKX2-5 Mutation and a Review of the Literature.Semantic proximity Read ↗

Novel NKX2-5 mutations responsible for congenital heart disease.Semantic proximity Read ↗

A novel NKX2.6 mutation associated with congenital ventricular septal defect.Semantic proximity Read ↗

Investigation of somatic NKX2-5 mutations in congenital heart disease.Semantic proximity Read ↗

Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations.Semantic proximity Read ↗

Human Genetics of Ventricular Septal Defect.Semantic proximity Read ↗

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

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