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

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作者
Juan Fan
Hua-Yun He
Huan-Huan Li
Pi-Liu Wu
Lei Tang
Bo-Yin Deng
Wen-Hui Dong
Jian-Hui Wang
机构
[1] Children’s Hospital of Chongqing Medical University,Department of Neonatology
[2] National Clinical Research Center for Child Health and Disorders,Department of Neonatology
[3] Ministry of Education Key Laboratory of Child Development and Disorders,Department of Neonatology
[4] Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity,Department of Pediatrics
[5] Chongqing Jiulongpo People’s Hospital,undefined
[6] Bishan Maternity & Child Hospital of Chongqing,undefined
[7] Affiliated Banan Hospital of Chongqing Medical University,undefined
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Single nucleotide polymorphism; UGT1A1; SLCO1B3; Neonatal hyperbilirubinemia;
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