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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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Wedi'i Gadw mewn:

Manylion Llyfryddiaeth
Prif Awdur:	Young Don Kim (Awdur)
Fformat:	Llyfr
Cyhoeddwyd:	Korean Society of Neonatology, 2024-02-01T00:00:00Z.
Pynciau:	article
Mynediad Ar-lein:	Connect to this object online.
Tagiau:	Ychwanegu Tag Dim Tagiau, Byddwch y cyntaf i dagio'r cofnod hwn!

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