A patient with novel ABCB11 gene mutations with phenotypic transition between BRIC2 and PFIC2
Author:
Publisher
Elsevier BV
Subject
Hepatology
Reference8 articles.
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2. Benign recurrent intrahepatic cholestasis type 2 is caused by mutations in ABCB11;van Mil;Gastroenterology,2005
3. Hepatocanalicular bile salt export pump deficiency in patients with progressive familial intrahepatic cholestasis;Jansen;Gastroenterology,1999
4. Benign recurrent intrahepatic cholestasis progressing to progressive familial intrahepatic cholestasis: low GGT cholestasis is a clinical continuum;van Ooteghem;J Hepatol,2002
5. Benign recurrent intrahepatic cholestasis in a Chinese girl;Lau;J Gastroenterol Hepatol,1989
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