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Article

Analyses of GATA4, NKX2.5, and TFAP2B genes in subjects from southern China with sporadic congenital heart disease.

Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology - 1 Jan 2000

Xiong Fu, Li Qian, Zhang Cuimei, Chen Youming, Li Ping, Wei Xiaofeng, Li Qiang, Zhou Wanjun, Li Liang, Shang Xuan, Xu Xiangmin

Abstract excerpt

BACKGROUND: Congenital heart disease is the most common birth defect in newborns in southern China. The germline mutations in GATA4, NKX2.5, and TFAP2B genes have been identified to be responsible for congenital heart disease. The frequency of GATA4, NKX2.5, and TFAP2B mutations in subjects with congenital heart disease in southern China and the correlation between their genotype and congenital heart disease...

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Share to GATA4 Transcription Factor
Share to Heart Defects, Congenital

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

Share to Homeobox Protein Nkx-2.5

Share to Homeodomain Proteins

Share to Infant, Newborn

Share to Mutation, Missense

Share to Sequence Homology, Amino Acid

Share to Transcription Factor AP-2

Source

Identifiers

PMID: 22959235
DOI: 10.1016/j.carpath.2012.07.001

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.

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