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Article

A novel variation of PLAGL1 in Chinese patients with isolated ventricular septal defect.

Genetic testing and molecular biomarkers - 1 Aug 2012

Xuan Chao, Wang Bin-Bin, Gao Ge, Bai Xiao-Yan, Yang Qin, Liu Xiao-Cheng, Jing Wen-Bin, Ma Xu, He Guo-Wei

Abstract excerpt

AIMS: Ventricular septal defect (VSD) is the most common congenital heart disease (CHD). A number of genetic studies have linked the gene of PLAGL1 to the etiology of CHD. The present study aimed to identify potential pathogenic mutations for PLAGL1 and to provide insights into the etiology of is...

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Source

Open in PubMed Open full text

Identifiers

PMID: 22784302
DOI: 10.1089/gtmb.2012.0003
PMCID: PMC3422556

Genes

PLAGL1
CLC

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-22784302-2026-09-04.1. Manifest publication-graph-cohort-2026-09-04.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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