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Article

GATA5 loss-of-function mutation responsible for the congenital ventriculoseptal defect.

Pediatric cardiology - 1 Mar 2013

Wei Dong, Bao Han, Zhou Ning, Zheng Gui-Fen, Liu Xing-Yuan, Yang Yi-Qing

Abstract excerpt

The ventriculoseptal defect (VSD) is the most common form of congenital heart disease and a leading noninfectious cause of infant mortality. Growing evidence demonstrates that genetic defects are associated with congenital VSD. Nevertheless, VSD is genetically heterogeneous, and the molecular basis for VSD in an overwhelming majority of patients remains unknown. In this study, the whole coding region of GATA5, a...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Heart Septal Defects, Ventricular

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Source

Identifiers

PMID: 22961344
DOI: 10.1007/s00246-012-0482-6

Genes

GATA5

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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