Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population

Abstract Background Severe neonatal hyperbilirubinemia could lead to kernicterus and neonatal death. This study aimed to analyze the association between single nucleotide polymorphisms in genes involved in bilirubin metabolism and the incidence of severe hyperbilirubinemia. Methods A total of 144 ne...

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Huvudupphov:	Juan Fan, Hua-Yun He, Huan-Huan Li, Pi-Liu Wu, Lei Tang, Bo-Yin Deng, Wen-Hui Dong, Jian-Hui Wang
Materialtyp:	Artigo
Språk:	Inglês
Utgiven:	BMC 2024-01-01
Serie:	BMC Pediatrics
Ämnen:	Single nucleotide polymorphism UGT1A1 SLCO1B3 Neonatal hyperbilirubinemia
Länkar:	https://doi.org/10.1186/s12887-024-04537-0
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