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...
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Korean Society of Neonatology
2024-02-01
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| Reeks: | Neonatal Medicine |
| Onderwerpen: | |
| Online toegang: | http://neo-med.org/upload/pdf/nm-2024-31-1-1.pdf |
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