Combined Effects of UGT1A1 and SLCO1B1 Variants on Chinese Adult Mild Unconjugated Hyperbilirubinemia
Author:
Publisher
Frontiers Media SA
Subject
Genetics (clinical),Genetics,Molecular Medicine
Reference32 articles.
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2. UGT1A1 sequence variants associated with risk of adult hyperbilirubinemia: a quantitative analysis;Chen;Gene,2014
3. Genetic Variations in Bilirubin Metabolism Genes and Their Association with Unconjugated Hyperbilirubinemia in Adults;Chiddarwar;Ann. Hum. Genet.,2017
4. Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias;Clarke;Clin. Chim. Acta.,1997
5. Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates;D'Silva;Gene,2014
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