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...
保存先:
| 第一著者: | |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Korean Society of Neonatology
2024-02-01
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| シリーズ: | Neonatal Medicine |
| 主題: | |
| オンライン･アクセス: | http://neo-med.org/upload/pdf/nm-2024-31-1-1.pdf |
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