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7. UGT1A1 gene mutations in Pakistani children suffering from inherited nonhemolytic unconjugated hyperbilirubinemias. Khan S, Irfan M, Sher G, Zubaida B, Alvi MA, Yasinzai M, Naeem M. Ann Hum Genet; 2013 Nov 16; 77(6):482-7. PubMed ID: 23992562 [Abstract] [Full Text] [Related]
8. Genotype of UGT1A1 and phenotype correlation between Crigler-Najjar syndrome type II and Gilbert syndrome. Maruo Y, Nakahara S, Yanagi T, Nomura A, Mimura Y, Matsui K, Sato H, Takeuchi Y. J Gastroenterol Hepatol; 2016 Feb 16; 31(2):403-8. PubMed ID: 26250421 [Abstract] [Full Text] [Related]
9. [Inherited disorders of bilirubin metabolism]. Rossi F, Francese M, Iodice RM, Falcone E, Vetrella S, Punzo F, De Vita S, Perrotta S. Minerva Pediatr; 2005 Apr 16; 57(2):53-63. PubMed ID: 15985997 [Abstract] [Full Text] [Related]
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