Article

Co-Inheritance of G6PD Deficiency and 211 G to A Variation of UGT1A1 in Neonates with Hyperbilirubinemia In Eastern Guangdong

2021-08-10

Abstract excerpt

<h4>Background: </h4> Glucose-6-phosphate dehydrogenase (G6PD) deficiency, which may manifest as neonatal hyperbilirubinemia, is the most prevalent erythrocytic enzyme-related disease in the world. <h4>Objective: </h4> To investigate the association between neonatal hyperbilirubinemia and co-inheritance of G6PD deficiency and 211 G to A variation of UGT1A1 in Chaozhou city of eastern Guangdong province, the effect...

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Literature Corpus work: f43202a0-765b-5459-bd62-dd6c0fbac1b5
DOI: 10.21203/rs.3.rs-745740/v1

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