Varaico: Literature-Extracted Genetic Variants

Gene:GATA4
Variant:p.H28Y
Back to variants list

GATA4

NM_001308093.3:p.H28Y

Associated Papers

In silico analysis of GATA4 variants demonstrates main contribution to congenital heart disease.

Abbasi S et al.

Journal of Cardiovascular and Thoracic Research, 2021

A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease.

Zhang X et al.

Plos One, 2016

27391137 (PubMed )
Supplement: pone.0158904.s003.pdf

Insights into the genetic structure of congenital heart disease from human and murine studies on monogenic disorders.

Prendiville T et al.

Cold Spring Harbor Perspectives in Medicine, 2014

Identification of functional mutations in GATA4 in patients with congenital heart disease.

Wang E et al.

Plos One, 2013

23626780 (PubMed )
Supplement: pone.0062138.s004.xlsx › information_of_all_mutations

Novel GATA4 mutations in patients with congenital ventricular septal defects.

Yang YQ et al.

Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2012

A novel GATA4 mutation responsible for congenital ventricular septal defects.

Wang J et al.

International Journal of Molecular Medicine, 2011

Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease.

Peng T et al.

Genetica, 2010

[Novel GATA4 mutations identified in patients with congenital atrial septal defects].

Liu XY et al.

Zhonghua Xin Xue Guan Bing Za Zhi, 2010

[Novel GATA4 mutations identified in patients with congenital heart disease].

Wang J et al.

Zhonghua Yi Xue Za Zhi, 2010

GATA4 mutations in Chinese patients with congenital cardiac septal defects.

Chen MW et al.

Pediatric Cardiology, 2010

[Association between GATA-4 mutations and congenital cardiac septal defects in Han Chinese patients].

Chen MW et al.

Zhonghua Xin Xue Guan Bing Za Zhi, 2009

Effect of Structural Changes in Proteins Derived from GATA4 Nonsynonymous Single Nucleotide Polymorphisms in Congenital Heart Disease.

Manjegowda DS et al.

Indian Journal of Pharmaceutical Sciences, 0

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."