[1] Functional analysis of ABCB4 mutations relates clinical outcomes of progressive familial intrahepatic cholestasis type 3 to the degree of MDR3 floppase activity.Gut. 2015 Jan;64(1):147-55.

[2] Functional defect of variants in the adenosine triphosphate-binding sites of ABCB4 and their rescue by the cystic fibrosis transmembrane conductance regulator potentiator, ivacaftor (VX-770).Hepatology. 2017 Feb;65(2):560-570.

[3] Bile salt-stimulated phospholipid efflux mediated by ABCB4 localized in nonraft membranes.J Lipid Res. 2013 May;54(5):1221-30.

[4] Two ABCB4 point mutations of strategic NBD-motifs do not prevent protein targeting to the plasma membrane but promote MDR3 dysfunction.Eur J Hum Genet. 2014 May;22(5):633-9.