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.

Riskin, Arieh; Bravdo, Yulia; Habib, Clair; Maor, Irit; Mousa, Julnar; Shahbarat, Sizett; Shahak, Elena; Shalata, Adel

Riskin, Arieh; Bravdo, Yulia; Habib, Clair; Maor, Irit; Mousa, Julnar; Shahbarat, Sizett; Shahak, Elena; Shalata, Adel.

Afiliación

Riskin A; Department of Neonatology, Bnai Zion Medical Center, Ruth & Bruce Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa 32000, Israel.
Bravdo Y; Department of Pediatrics, Bnai Zion Medical Center, Ruth & Bruce Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa 32000, Israel.
Habib C; Department of Pediatrics, Bnai Zion Medical Center, Ruth & Bruce Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa 32000, Israel.
Maor I; Biochemistry Laboratory, Bnai Zion Medical Center, Ruth & Bruce Rappaport Faculty of Medicine, Technion, Israel Institute of Technology, Haifa 32000, Israel.
Mousa J; 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.
Shahbarat S; 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.
Shahak E; 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.
Shalata A; 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.

Children (Basel) ; 10(7)2023 Jul 06.

Article en En | MEDLINE | ID: mdl-37508669

Palabras clave

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)

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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Children (Basel) Año: 2023 Tipo del documento: Article País de afiliación: Israel

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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Children (Basel) Año: 2023 Tipo del documento: Article País de afiliación: Israel