Copyright
©The Author(s) 1998.
World J Gastroenterol. Jun 15, 1998; 4(3): 185-191
Published online Jun 15, 1998. doi: 10.3748/wjg.v4.i3.185
Published online Jun 15, 1998. doi: 10.3748/wjg.v4.i3.185
Disease | Gene |
Wilson disease | Cu-transporting ATPase |
Hereditary hemochromatosis | HFE |
Crigler-Najjar syndrome | UDP-glucuronosyltransferase |
Dubin-Johnson syndrome | cMOAT |
Benign recurrent intrahepatic cholestasis | P-type ATPase |
Progressive familial Intrahepatic Cholestasis Type 1 | P-type ATPase |
Polypeptide | Function | Reference |
NS3 protease domain | Protease that cleaves HCV polyprotein at several locations | 75, 76 |
NS4A (complexed to NS3) | Cofactor for NS3 protease | 76 |
NS3 RNA helicase domain | Unwinds viral RNA | 77, 78 |
- Citation: Worman HJ, Lin F, Mamiya N, Mustacchia PJ. Molecular biology and the diagnosis and treatment of liver diseases. World J Gastroenterol 1998; 4(3): 185-191
- URL: https://www.wjgnet.com/1007-9327/full/v4/i3/185.htm
- DOI: https://dx.doi.org/10.3748/wjg.v4.i3.185