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

• Hoofdauteurs: Jia-Xin Xu (Auteur), Fen Lin (Auteur), Zi-Kai Chen (Auteur), Zhao-Yun Luo (Auteur), Xiao-Fen Zhan (Auteur), Jiao-Ren Wu (Auteur), Yu-Bin Ma (Auteur), Jian-Dong Li (Auteur), Li-Ye Yang (Auteur)
• Formaat: Boek
• Gepubliceerd in: BMC, 2021-12-01T00:00:00Z.
• Onderwerpen: article
• Online toegang: 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...