UGT1A1*28 gene polymorphism was not associated with the risk of neonatal hyperbilirubinemia: a meta-analysis
Author:
Affiliation:
1. Department of Neonatology, Linyi People’s Hospital, Linyi, China
2. Department of Pediatrics, Linyi People’s Hospital, Linyi, China
Publisher
Informa UK Limited
Subject
Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health
Link
https://www.tandfonline.com/doi/pdf/10.1080/14767058.2019.1702962
Reference34 articles.
1. Developmental, Genetic, Dietary, and Xenobiotic Influences on Neonatal Hyperbilirubinemia
2. Importance of UDP-Glucuronosyltransferase 1A1 Expression in Skin and Its Induction by UVB in Neonatal Hyperbilirubinemia
3. Association of neonatal hyperbilirubinemia in breast-fed infants with UGT1A1 or SLCOs polymorphisms
4. Humanized UGT1 Mice, Regulation of UGT1A1, and the Role of the Intestinal Tract in Neonatal Hyperbilirubinemia and Breast Milk-Induced Jaundice
5. Association between uridin diphosphate glucuronosylotranserase 1A1 (UGT1A1) gene polymorphism and neonatal hyperbilirubinemia
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