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Article

Analysis of RTN4 3'UTR insertion/deletion polymorphisms in ventricular septal defect in a Chinese Han population.

DNA and cell biology - 1 May 2011

Chen Yu, Zhou Bin, Li Hui, Peng Ying, Wang Yanyun, Rao Li

Abstract excerpt

Congenital heart disease is the most common type of birth defect and the leading cause of infant mortality in the first year of life. Ventricular septal defect (VSD) is one of the most general congenital heart defects and is a defect in the wall between the right and left ventricles of the heart. The pathogenesis of VSD has been extensively investigated for many years, but it remains uncertain. To determine...

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Identifiers

PMID: 21166502
DOI: 10.1089/dna.2010.1116

Genes

RTN4

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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