Molecular biology of glucose-6-phosphate dehydrogenase and UDP-glucuronosyltransferase 1A1 in the development of neonatal unconjugated hyperbilirubinemia-Reference-Cited by-同舟云学术

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

Published:2024-09 Issue:5 Volume:65 Page:419-426
ISSN:1875-9572
Container-title:Pediatrics & Neonatology
language:en
Short-container-title:Pediatrics & Neonatology

Author:

Hung Yi-Li,Chang Pi-Feng^ORCID,Huang Ching-Shan^ORCID

Publisher

Elsevier BV

Reference52 articles.

1. Neonatal jaundice;Ansong-Assoku,2022

2. Clinical and genetic etiologies of neonatal unconjugated hyperbilirubinemia in the China neonatal genomes project;Mei;J Pediatr,2022

3. Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia;Vulliamy;Proc Natl Acad Sci U S A,1988

4. Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA;Poggi;Biochem J,1990

5. Glucose-6-Phosphate dehydrogenase deficiency and neonatal hyperbilirubinemia: insights on pathophysiology, diagnosis, and gene variants in disease heterogeneity;Lee;Front Pediatr,2022

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