The Genetics of Glucose-6-Phosphate-Dehydrogenase (G6PD) and Uridine Diphosphate Glucuronosyl Transferase 1A1 (UGT1A1) Promoter Gene Polymorphism in Relation to Quantitative Biochemical G6PD Activity Measurement and Neonatal Hyperbilirubinemia.

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作者： Arieh,Riskin ^[1] ; Yulia,Bravdo ^[2] ; Clair,Habib ^[2] ; Irit,Maor ^[3] ; Julnar,Mousa ^[4] ; Sizett,Shahbarat ^[4] ; Elena,Shahak ^[4] ; Adel,Shalata ^[4]

作者单位： Department of Neonatology, Bnai Zion Medical Center, Ruth & Bruce Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa 32000, Israel. ^[1] Department of Pediatrics, Bnai Zion Medical Center, Ruth & Bruce Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa 32000, Israel. ^[2] Biochemistry Laboratory, Bnai Zion Medical Center, Ruth & Bruce Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa 32000, Israel. ^[3] The Simon Winter Institute for Human Genetics, Bnai Zion Medical Center, Ruth & Bruce Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa 32000, Israel. ^[4]

关键词 G6PD deficiency G6PD enzyme activity Mediterranean mutation UGT1A1 promoter polymorphism genotype glucose-6-phosphate dehydrogenase (G6PD)neonatal hyperbilirubinemia (NHB)number of TA repeats phenotype uridine diphosphate glucuronosyl transferase 1A1 (UGT1A1)

DOI 10.3390/children10071172

PMID 37508669

发布时间 2023-07-31

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Children (Basel, Switzerland)

2023年10卷7期

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The Genetics of Glucose-6-Phosphate-Dehydrogenase (G6PD) and Uridine Diphosphate Glucuronosyl Transferase 1A1 (UGT1A1) Promoter Gene Polymorphism in Relation to Quantitative Biochemical G6PD Activity Measurement and Neonatal Hyperbilirubinemia.

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The Genetics of Glucose-6-Phosphate-Dehydrogenase (G6PD) and Uridine Diphosphate Glucuronosyl Transferase 1A1 (UGT1A1) Promoter Gene Polymorphism in Relation to Quantitative Biochemical G6PD Activity Measurement and Neonatal Hyperbilirubinemia.

Children (Basel, Switzerland)

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Children (Basel, Switzerland)

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