GATA6 Mutation: A Rare Genetic Cause of Hepatobiliary Disease

J Pediatr Gastroenterol Nutr. 2017 May;64(5):e134-e135. doi: 10.1097/MPG.0000000000000691.

Authors

Sandra Ferreira¹, David Devadason, Louise Denvir, Anna Seale, Girish Gupte

Affiliation

¹ *Liver Unit, Coimbra's Paediatric Hospital, Portugal †Department of Paediatric Gastroenterology ‡Queens Medical Centre, Nottingham University Hospitals §Department of Cardiology ||Liver Unit (and small bowel transplantation), Birmingham's Children Hospital, UK.

PMID: 25564821
DOI: 10.1097/MPG.0000000000000691

No abstract available

Publication types

Case Reports

MeSH terms

Biliary Tract Diseases / genetics*
Cholestasis / etiology
Female
GATA6 Transcription Factor / genetics*
Humans
Infant, Newborn
Jaundice, Neonatal / etiology
Liver Diseases / genetics*
Mutation

Substances

GATA6 Transcription Factor
GATA6 protein, human