Co-inheritance of G6PD Deficiency and 211 G to a Variation of UGT1A1 in Neonates with Hyperbilirubinemia in Eastern Guangdong.
BMC Pediatrics（2021）
关键词
Neonatal hyperbilirubinemia,Glucose-6-phosphate dehydrogenase deficiency,Uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1)
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