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先天性非溶血性黄疸分子生物学研究进展 被引量:2

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出处 《临床肝胆病杂志》 CAS 北大核心 2001年第3期142-143,共2页 Journal of Clinical Hepatology
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  • 1[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[2]Clarke DJ, Moghrabi N, Monaghan G, et al. Genetic defects of the UDP glucuronosyltransferase-1 (UGT1)gene that cause familial nonhaemolytic unconjugated hyperbilirubinaemias [ J ]. Clinica Chimica Acta, 1997,266(1):63.
  • 3[3]Bosma PJ, Chowdhury JR, Bakker C, et al. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert' s syndrome[J ]. N Eng J Med, 1995,333 (18): 1171.
  • 4[4]Monaghan G, Ryan M, Seddon R, et al. Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome[J]. Lancet, 1996,347 (9001 ): 578.
  • 5[5]Gantla S, Bakker CT, Deocharan B, et al. Splice-site mutations: a novel genetic mechanism of Crigler-Najjar syndrome type 1 [J ]. Am J Hum Genet, 1998,62 (3): 585.
  • 6[6]Paulusma CC, Kool M, Bosma PJ, et al A mutation in the human canalicular multispecific organic anion transporter gene causes the Dubin-Johnson syndrome [J]. Hepatology, 1997,25(6): 1539.

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