Molecular biology of glucose-6-phosphate dehydrogenase and UDP-glucuronosyltransferase 1A1 in the development of neonatal unconjugated hyperbilirubinemia

Glucose-6-phosphate dehydrogenase (G6PD) deficiency and variants of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene are the most common genetic causes of neonatal unconjugated hyperbilirubinemia (NUH). In this review, we searched PubMed for articles on the genetic causes of NUH published before De...

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Bibliographic Details
Published in:	Pediatrics and Neonatology
Main Authors:	Yi-Li Hung, Pi-Feng Chang, Ching-Shan Huang
Format:	Article
Language:	English
Published:	Elsevier 2024-09-01
Subjects:	Glucose-6-phosphate dehydrogenase Neonatal unconjugated hyperbilirubinemia UDP-Glucuronosyltransferase 1A1
Online Access:	http://www.sciencedirect.com/science/article/pii/S1875957224000202

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