Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Hyperbilirubinemia and UGT1A6[original query] |
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Combined polymorphisms in UDP-glucuronosyltransferases 1A1 and 1A6: implications for patients with Gilbert's syndrome. Journal of hepatology 2003 Jan 38 (1): 3-8. Peters Wilbert H M, te Morsche Rene H M, Roelofs Hennie M |
Gilbert syndrome redefined: a complex genetic haplotype influences the regulation of glucuronidation. Hepatology (Baltimore, Md.) 2012 Jun 55 (6): 1912-21. Ehmer Ursula, Kalthoff Sandra, Fakundiny Bastian, Pabst Brigitte, Freiberg Nicole, Naumann Ronald, Manns Michael P, Strassburg Christian |
Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant Article. Medicine 2015 Jun 94 (22): e925. Oussalah Abderrahim, Bosco Paolo, Anello Guido, Spada Rosario, Guéant-Rodriguez Rosa-Maria, Chery Céline, Rouyer Pierre, Josse Thomas, Romano Antonino, Elia Maurizzio, Bronowicki Jean-Pierre, Guéant Jean-Lou |
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