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

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)...

Source: BMC Medical Genetics - November 6, 2020 Category: Genetics & Stem Cells Authors: Zijin Li, Li Song and Lihong Hao Tags: Research article Source Type: research