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

[Mutations in the GATA4 gen in patients with non-syndromic congenital heart disease].

Investigacion clinica - 1 Sept 2014

Orjuela Quintero Diana Carolina, Núñez Federico, Caicedo Víctor, Pachón Sonia, Salazar Salazar Marleny

Abstract excerpt

Congenital heart diseases are defined as any heart or large vessel structural abnormality resulting from abnormal embryonic development, usually described between the 3rd and 10th week of gestation. They comprise the second cause of death in children under a year of age in Colombia, with a prevalence of 7.5-9.5 per 1,000 births, including live and still births. We analyzed 33 heart tissue samples collected at the...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Child, Preschool
Share to Colombia

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to GATA4 Transcription Factor

Share to Heart Defects, Congenital

Share to Infant

Share to Infant, Newborn

Share to Polymorphism, Genetic

Source

Identifiers

PMID: 25272520

Genes

GATA4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

[Mutations in the GATA4 gen in patients with non-syndromic congenital heart disease].PMID 25272520Read ↗

[Novel GATA4 mutations identified in patients with congenital heart disease].Semantic proximity Read ↗

GATA4 specific nonsynonymous single-nucleotide polymorphisms in congenital heart disease patients of Mysore, India.Semantic proximity Read ↗

Personalized Genetic Diagnosis of Congenital Heart Defects in NewbornsSemantic proximity Read ↗

[Novel GATA4 mutations identified in patients with congenital atrial septal defects].Semantic proximity Read ↗

Novel pathogenic GATA6 variant associated with congenital heart disease, diabetes mellitus and necrotizing enterocolitisSemantic proximity Read ↗

A novel mutation in exon 1 of GATA4 in Egyptian patients with congenital heart disease.Semantic proximity Read ↗

Prevalence and spectrum of GATA5 mutations associated with congenital heart diseaseSemantic proximity Read ↗

GATA4 screening in Iranian patients of various ethnicities affected with congenital heart disease: Co‐occurrence of a novel de novo translocation (5;7) and a likely pathogenic heterozygous GATA4 mutation in a family with autosomal dominant congenital heart diseaseSemantic proximity Read ↗

Functional mutant GATA4 identification and potential application in preimplantation diagnosis of congenital heart diseases.Semantic proximity Read ↗

<i>GATA4</i> sequence variants in patients with congenital heart diseaseSemantic proximity Read ↗

c.620C>T mutation in GATA4 is associated with congenital heart disease in South India.Semantic proximity Read ↗

Whole-exome sequencing identifies a novel mutation in GATA4 gene to be congenital heart defects and arrhythmia in a Chinese familySemantic proximity Read ↗

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