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Genetic Interactions in the Pathogenesis of Neonatal Hyperbilirubinemia: Gilbert's Syndrome and Glucose-6-Phosphate Dehydrogenase Deficiency

✍ Scribed by Kaplan, MB, Michael


Book ID
110051459
Publisher
Nature Publishing Group
Year
2001
Tongue
English
Weight
121 KB
Volume
21
Category
Article
ISSN
1300-5251

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Glucose-6-phosphate dehydrogenase defici
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## Abstract In this study, we investigated whether glucose‐6‐phosphate dehydrogenase (G6PD) promoter mutations are responsible for G6PD deficiency. We analysed the G6PD proximal promoter and the 5β€² untranslated region (UTR) in 65 G6PD‐deficient individuals, in which no mutations have been found in