Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome
Author:
Affiliation:
1. Department of Pediatrics; Shiga University of Medical Science; Otsu Shiga Japan
2. Department of Health and Nutrition; Nagoya Bunri University; Inazawa Aichi Japan
Funder
Ministry of Education, Science, and Culture of Japan
Publisher
Wiley
Subject
Gastroenterology,Hepatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/jgh.13071/fullpdf
Reference33 articles.
1. Congenital familial nonhemolytic jaundice with kernicterus;Crigler;Pediatrics,1952
2. La cholémie simple familiale;Gilbert;Sem. Med.,1901
3. Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate glucuronosyltransferase gene;Maruo;Pediatrics,2000
4. Bilirubin uridine diphosphate-glucuronosyltransferase variation is a genetic basis of breast milk jaundice;Maruo;J. Pediatr.,2014
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