Associated Papers
Whole exome sequencing identifies novel inherited genetic variants in tetralogy of Fallot.
Pan Y et al.
Journal of Thoracic Disease, 2022
In silico analysis of GATA4 variants demonstrates main contribution to congenital heart disease.
Abbasi S et al.
Journal of Cardiovascular and Thoracic Research, 2021
Mutation Screening of Gata4 Gene in CTD Patients Within Chinese Han Population.
Liu Y et al.
Pediatric Cardiology, 2017
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
[A novel GATA4 mutation leading to congenital ventricular septal defect].
Yang YQ et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2010
Mutational analysis of the GATA4 gene in Chinese men with nonobstructive azoospermia.
Zhang X et al.
Asian Journal of Andrology, 0
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