The role of UGT1A1 (c.-3279 T > G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility

The role of UGT1A1 (c.-3279 T > G) gene polymorphisms in neonatal hyperbilirubinemia susceptibility

Abstract Background Neonatal hyperbilirubinemia (NNH) is a common disease in newborns. This research study aimed to assess the associations between uridine diphospho-glucuronate-glucuronosyltransferase 1A1 (UGT1A1, c.-3279 T > G) polymorphisms and NNH risk. Methods We searched PubMed, the Cochran...

Full description

Bibliographic Details
Main Authors: Zijin Li, Li Song, Lihong Hao
Format: Article
Language:English
Published: BMC 2020-11-01
Series:BMC Medical Genetics
Subjects:
UGT1A1
Neonatal hyperbilirubinemia
Neonatal jaundice
C.-3279 T > G
Polymorphism
Online Access:http://link.springer.com/article/10.1186/s12881-020-01155-2

Internet

http://link.springer.com/article/10.1186/s12881-020-01155-2

Similar Items