UGT1A1 (TA)n promoter polymorphism- A new case of a (TA)8 allele in Caucasians, Blood Cells, Molecules and Diseases, vol.38, pp.78-82, 2007. ,
Identification of a Defect in the UGT1A1 Gene Promoter and Its Association with Hyperbilirubinemia, Biochemical and Biophysical Research Communications, vol.292, issue.2, pp.492-497, 2002. ,
DOI : 10.1006/bbrc.2002.6683
Chromosomal localization, structure and regulation of the UGT2 B17 gene, encoding a steroid metabolizing enzyme, DNA. Cell. Biol, vol.16, pp.1143-1155, 1996. ,
The UDP glycosyltransferase gene superfamily: recommended nomenclature update based on evolutionary divergence, Pharmacogenetics, vol.7, issue.4, pp.255-269, 1997. ,
DOI : 10.1097/00008571-199708000-00001
The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome, New England Journal of Medicine, vol.333, issue.18, pp.1171-1175, 1995. ,
DOI : 10.1056/NEJM199511023331802
Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler???Najjar syndrome type II, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, vol.1406, issue.3, pp.267-273, 1998. ,
DOI : 10.1016/S0925-4439(98)00013-1
Hepatic Bilirubin UDP-Glucuronyl Transferase Activity in Liver Disease and Gilbert's Syndrome, New England Journal of Medicine, vol.280, issue.23, pp.1266-1271, 1969. ,
DOI : 10.1056/NEJM196906052802303
Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type I patient., Journal of Clinical Investigation, vol.90, issue.1, 1992. ,
DOI : 10.1172/JCI115829
Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes, Haematologica, vol.84, pp.150-157, 1999. ,