Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy
Type of publication:
Matching Publication
Published in:
Best Practice & Research in Clinical Gastroenterology
Date of publication:
2010/10
Link to publication:
Status of the publication:
Published/accepted
Theme:
Progressive familial intrahepatic cholestasis (PFIC) type 1, 2 and 3 are due to mutations in ATP8B1, ABCB11 and ABCB4, respectively. Each of these genes encodes a hepatocanalicular transporter, which is essential for the proper formation of bile.
Theme:
Pages:
2010; 24 (5): 541-553
DOI:
10.1016/j.bpg.2010.07.010