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良性复发性肝内胆汁淤积

蔡中起 徐惠

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良性复发性肝内胆汁淤积

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  • 中图分类号: R575

  • [1]De Konning TJ, Sandekujil LA, De Schryver JEAR, et al.Autosomal-recessive inheritance of benign recurrent intrahepatic cholestasis[J].AmJ Med Genet, 1995, 52 (2) ∶479-482.
    [2]Brenard R, Geubel AP, Benhamou JP Benign recurrent intrahepaticcholestasis[J].J Clin Gastroenterol, 1989, 11 (3) ∶564-568.
    [3]Carleton VEH, Kinsley AS, Freimer NB.Mapping of a locus for progres-sive familial intrahepatic cholestasis (Byler disease) to 18q21-q22, thebenign recurrent intrahepatic gene[J].Hum Mol Genet, 1995, 6 (7) ∶1049-1053.
    [4]Oude Elferink RPJ, Van Berge Henegouwen GP.Cracking the geneticcode for benign recurrent and progressive familial intrahepatic cholestasis[J].J Hepatol, 1998, 29 (2) ∶317-320.
    [5]Van Mil SWC, Klomp LWJ, Bull LN, et al.FIC1 disease∶a spectrum ofintrahepatic cholestic diseases[J].Semin Liver Dis, 2003, 21 (4) ∶535-543.
    [6]Eppens EF, Van Mil SWC, de Vree JML, et al.FIC1, the protein af-fected in two form of hereditary cholestasis, is localized in the cholangio-cyte and the canalicular membrane of the hepatocyte[J].J Hepatol, 2001, 35 (2) ∶436-443.
    [7]Eiberg H, Nielsen I-M.Linkage of cholestasis familiaris groenlandica/Byler-like disease to chromosome 18[J].Int J Circumpolar Health, 2000, 59 (1) ∶57-62.
    [8]Klomp LMJ, Bull LN, Kinsley AS, et al.A missense mutation is associ-ated with Greeland familial cholestasis[J].Hepatology, 2000, 32 (6) ∶1337-1342.
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  • 出版日期:  2006-01-20
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