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[1]Iyanagi T, Emi Y, Ikushiro S.Biochemical and molecular aspects of genetic disorders of bilirubin metabolism [J].Biochim Biophys Acta, 1998, 1407 (3) ∶173. [][2 ]ClarkeDJ, MoghrabiN , MonaghanG , etal.GeneticdefectsoftheUDPglucuronosyltransferase 1 (UGT1) genethatcausefamilialnon haemolyticunconjugatedhyperbilirubinaemias [J] .ClinicaChimicaActa, 1997, 2 6 6 (1) ∶6 3 . [3]BosmaPJ , ChowdhuryJR , BakkerC , etal.ThegeneticbasisofthereducedexpressionofbilirubinUDP glucuronosyltransferase 1inGilbert’ssyndrome[J] .NEngJMed , 1995 , 333 (18) ∶1171. [4]MonaghanG , RyanM , SeddonR , etal.GeneticvariationinbilirubinUDP glucuronosyltransferasegenepromoterandGilbert’ssyndrome[J] .Lancet , 1996 , 347 (90 0 1) ∶5 78. [][5 ]GantlaS , BakkerCT , DeocharanB , etal.Splice sitemutations:anovelgeneticmechanismofCrigler Najjarsyndrometype 1[J] .AmJHumGenet, 1998, 6 2 (3) ∶5 85 . [][6 ]PaulusmaCC , KoolM , BosmaPJ , etalAmutationinthehumancanalicularmultispecificorganicaniontransportergenecausestheDubin Johnsonsyndrome [J] .Hepatology , 1997, 2 5 (6 ) ∶15 39. -
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