1Baussan C, Cresteil D, Gonzales E, et al. Genetic cholestatic liver diseases., the example of progressive familial intrahepatic cholestasis and related disorders. Acta Gastroenterol Belg, 2004, 67: 179-183.
2Bull LN, van Eijk MJ, Pawlikowska L, et al. A gene encoding a P type ATPase mutated in two forms of hereditary cholestasis. Nat Genet, 1998,48:219-224.
3Strautnieks SS, Bull LN, Knisely AS, et al. A gene encoding a liver speci{ic ABC transporter is mutated in progressive {ami|ial intrahepatic cholestasis. Nat Genet, 1998,20 : 233 238.
4Kagalwalla AF, AI Amir AR, Khalifa A, et al. Progressive familial intrahepatic cholestasis (Byler's disease) in Arab children. Ann Trop Paediatr, 1995,15:321-327.
5Chen HL, Chang PS, Hsu HC, et al. FIC1 and BSEP defects in Taiwan Residents patients with chronic intrahepatic cholestasis with low gamma-glutamyltranspeptidase levels. J Pediatr, 2002, 140 : 119 /24.
6Liu LY, Wang XH, Wang ZI., et al. Characterization of ATP8B1 gene mutations and a hot-linked mutation found in Chinese children with progressive intrahepatic cholestasis and ow GGT. J Pediatr Gastroenterol Nutr, 2010, 50..:79 183.
7Folmer DE, Elferink RP, Paulusma CC. P4 ATPases lipid flippases and their role in disease. Bioehim Biophys Acta, 2009, 1791:628-635.
8Hohhuis JC, Levine TP. Lipid traffic: floppy drives and a super highway. Nat Rev Mol Cell Biol, 2005, 6:209 22{).
9Zachowski A. Phospholipids in animal eukaryotic membranes: transverse asymmetry and movement. Biochem J, 1993,294 : 1 14.
10Devaux PF, Lopez-Montero I, Bryde S. Proteins involved in lipid translocation in eukaryotic cells. Chem Phys I.ipids, 2006, 141: 119-132.
