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Article

The NFKB1 -94 ATTG insertion/deletion polymorphism (rs28362491) contributes to the susceptibility of congenital heart disease in a Chinese population.

Gene - 10 Mar 2013

Zhang Danyan, Li Lianbing, Zhu Yijian, Zhao Letian, Wan Ling, Lv Jing, Li Xinsheng, Huang Pei, Wei Li, Ma Mingfu

Abstract excerpt

Congenital heart disease (CHD) is the most frequently occurring congenital disorder in newborns and is the most frequent cause of infant death from birth defects. Human genetic studies have identified that numerous genes encoding transcription factors that regulate specific events in heart development are responsible for inherited and sporadic CHD. Nuclear factor-kappa B (NF-κB) is a major transcription regulator...

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Identifiers

PMID: 23299027
DOI: 10.1016/j.gene.2012.12.078

Genes

NFKB1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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