UGT1A1 and BLVRA allele and genotype variants in neonatal patients with hyperbilirubinemia in southern China

Abstract We explore the allele and genotype distribution of UGT1A1 and BLVRA variants in individuals affected by neonatal hyperbilirubinemia in southern China. Blood specimens were collected from 240 neonates: 126 cases of hyperbilirubinemia and 114 healthy controls. Serum levels of total protein, a...

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Detalhes bibliográficos

Principais autores:	XiuJu Liu, Chao Zhang, LiWen Chen, ShuYan Liu, ZhenWen Zhou
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Nature Portfolio 2024-10-01
Colecção:	Scientific Reports
Assuntos:	Biliverdin reductase A (BLVRA) Neonatal hyperbilirubinemia (NHB) Single nucleotide polymorphism (SNP) Uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1)
Acesso em linha:	https://doi.org/10.1038/s41598-024-77499-z
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