[1]Soroka CJ, Boyer JL. Biosynthesis and trafficking of the bile salt export pump, BSEP: therapeutic implications of BSEP mutations. Mol Aspects Med, 2014, 37: 3-14
[2]van der Woerd WL, van Mil SW, Stapelbroek JM, et al. Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy. Best Pract Res Clin Gastroenterol, 2010, 24(5): 541-553
[3]邓宝成, 刘沛. 进行性家族性肝内胆汁淤积症的研究现状. 临床肝胆病杂志, 2015, 31(10): 1599-1604
[4]徐铭益, 陆伦根. 良性复发性肝内胆汁淤积诊治进展. 中国医学前沿杂志(电子版), 2015, (4): 5-9
[5]Liu LY, Wang XH, Lu Y, et al. Association of variants of ABCB11 with transient neonatal cholestasis. Pediatr Int, 2013, 55(2): 138-144
[6]van Mil SW, van der Woerd WL, van der Brugge G, et al. Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11. Gastroenterology, 2004, 127(2): 379–384
[7]Strautnieks SS, Byrne JA, Pawlikowska L, et al. Severe bile salt export pump defificiency: 82 different ABCB11 mutations in 109 families. Gastroenterology, 2008, 134(4): 1203–1214 |
