Mutation specific drug therapy for progressive familial or benign recurrent intrahepatic cholestasis: A new tool in a near future?

Emmanuel Gonzales, Emmanuel Jacquemin
2010 Journal of Hepatology  
Deficiency in P-type ATP8B1 is a severe and clinically
doi:10.1016/j.jhep.2010.03.012 pmid:20537422 fatcat:ltehza5qlzevzpmal35cjfehxm