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3. Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype. Kadakol A; Ghosh SS; Sappal BS; Sharma G; Chowdhury JR; Chowdhury NR Hum Mutat; 2000 Oct; 16(4):297-306. PubMed ID: 11013440 [TBL] [Abstract][Full Text] [Related]
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10. [Type I Crigler Najjar syndrome in Tunisia: a study of 30 cases]. Aloulou H; Ben Thabet A; Khanfir S; Ben Mansour L; Chabchoub I; Labrune P; Kammoun T; Hachicha M Tunis Med; 2010 Oct; 88(10):707-9. PubMed ID: 20890816 [TBL] [Abstract][Full Text] [Related]
11. Unconjugated bilirubin and an increased proportion of bilirubin monoconjugates in the bile of patients with Gilbert's syndrome and Crigler-Najjar disease. Fevery J; Blanckaert N; Heirwegh KP; Préaux AM; Berthelot P J Clin Invest; 1977 Nov; 60(5):970-9. PubMed ID: 409736 [TBL] [Abstract][Full Text] [Related]
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15. Crigler-Najjar Type 1 syndrome: absence of hepatic bilirubin UDP-glucuronyl transferase activity and therapeutic responses to light. Farrell GC; Gollan JL; Stevens SM; Grierson JM Aust N Z J Med; 1982 Aug; 12(4):280-5. PubMed ID: 6814411 [TBL] [Abstract][Full Text] [Related]
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