Should We Consider Mutation Analysis in Evaluating the Prolonged Jaundice of Newborn Infants?
Purpose Uridine diphosphate glucuronosyltransferase 1A isoform 1 (UGT1A1) is a crucial enzyme in bilirubin metabolism. Mutations in this gene cause prolonged unconjugated hyperbilirubinemia in infants. This study aimed to investigate the prevalence of UGT1A1 mutations and their association with prol...
Na minha lista:
| Autor principal: | |
|---|---|
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Korean Society of Neonatology
2024-02-01
|
| coleção: | Neonatal Medicine |
| Assuntos: | |
| Acesso em linha: | http://neo-med.org/upload/pdf/nm-2024-31-1-1.pdf |
| Tags: |
Sem tags, seja o primeiro a adicionar uma tag!
|