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Article

Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease.

European journal of medical genetics - 1 Oct 2014

Zhao Lan, Ni Shi-Hong, Liu Xing-Yuan, Wei Dong, Yuan Fang, Xu Lei, Xin-Li, Li Ruo-Gu, Qu Xin-Kai, Xu Ying-Jia, Fang Wei-Yi, Yang Yi-Qing, Qiu Xing-Biao

Abstract excerpt

Congenital heart disease (CHD) is the most common form of birth defect and is the most prevalent non-infectious cause of infant death. A growing body of evidence documents that genetic defects are involved in the pathogenesis of CHD. However, CHD is a genetically heterogeneous disease and the genetic basis underpinning CHD in an overwhelming majority of patients remain unclear. In this study, the coding exons and...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 25195019
DOI: 10.1016/j.ejmg.2014.08.005

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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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