Gene Mutation in Neonatal Jaundice – Mutations in UGT1A1 and OATP2 Genes
Author:
Funder
N/A
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12098-016-2064-8.pdf
Reference10 articles.
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2. Kaga A, Ohkubo Y, Watanabe Y, et al. Development of icterus gravis in a preterm infant with G71R UGT1A1 polymorphism. BMC Res Notes. 2013;6:51.
3. American Academy of Pediatrics Subcommittee on Hyperbilirubinemia. Magnement of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation. Pediatrics. 2004;114:297–316.
4. Huang MJ, Kua KE, Teng HC, Tang KS, Weng HW, Huang CS. Risk factors for severe hyperbilirubinemia in neonates. Pediatr Res. 2004;56:682–9.
5. Fujiwara R, Chen S, Karin M, Tukey RH. Reduced expression of UGT1A1 in intestines of humanized UGT1 mice via inactivation of NF-κB leads to hyperbilirubinemia. Gastroenterology. 2012;142:109–18.e2.
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