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Article

GATA6 Mutation: A Rare Genetic Cause of Hepatobiliary Disease.

Journal of pediatric gastroenterology and nutrition - 1 May 2017

Ferreira Sandra, Devadason David, Denvir Louise, Seale Anna, Gupte Girish

Abstract excerpt

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Share to Cholestasis
Share to GATA6 Transcription Factor
Share to GATA6 gene
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Jaundice, Neonatal

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Identifiers

PMID: 25564821
DOI: 10.1097/MPG.0000000000000691

Genes

GATA6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

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GATA6 Mutation: A Rare Genetic Cause of Hepatobiliary Disease.PMID 25564821Read ↗

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Novel pathogenic GATA6 variant associated with congenital heart disease, diabetes mellitus and necrotizing enterocolitisSemantic proximity Read ↗

An animal model recapitulates human hepatic diseases associated with GATA6 mutations.Semantic proximity Read ↗

GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrumSemantic proximity Read ↗

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The Identification of a Novel Pathogenic Variant in the GATA6 Gene in a Child with Neonatal Diabetes.Semantic proximity Read ↗

GATA6 inactivating mutations are associated with heart defects and, inconsistently, with pancreatic agenesis and diabetes.Semantic proximity Read ↗

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Multiple roles and regulatory mechanisms of the transcription factor GATA6 in human cancersSemantic proximity Read ↗

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