Co-inheritance of G6PD deficiency and 211 G to a variation of UGT1A1 in neonates with hyperbilirubinemia in eastern Guangdong

• Main Authors: Jia-Xin Xu (Author), Fen Lin (Author), Zi-Kai Chen (Author), Zhao-Yun Luo (Author), Xiao-Fen Zhan (Author), Jiao-Ren Wu (Author), Yu-Bin Ma (Author), Jian-Dong Li (Author), Li-Ye Yang (Author)
• Format: Book
• Published: BMC, 2021-12-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background Glucose-6-phosphate dehydrogenase (G6PD) deficiency, which may manifest as neonatal hyperbilirubinemia, is the most prevalent erythrocytic enzyme-related disease in the world. Objective To investigate the association between neonatal hyperbilirubinemia and co-inheritance of G6PD...