Genetic variations of the NPC1L1 gene associated with hepatitis C virus (HCV) infection and biochemical characteristics of HCV patients in China
Author(s) -
A.-Mei Zhang,
Chenglin Zhang,
Yuzhu Song,
Ping Zhao,
Yue Feng,
Binghui Wang,
Zheng Li,
Li Liu,
Xueshan Xia
Publication year - 2016
Publication title -
international journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.278
H-Index - 89
eISSN - 1878-3511
pISSN - 1201-9712
DOI - 10.1016/j.ijid.2016.10.007
Subject(s) - haplotype , single nucleotide polymorphism , genotype , hepatitis c virus , biology , hepatocellular carcinoma , virology , allele , population , hepatitis c , immunology , virus , gene , genetics , medicine , environmental health
About 2% of the world population is infected with hepatitis C virus (HCV), a leading cause of hepatic cirrhosis and hepatocellular carcinoma. The Niemann-Pick C1-like 1 cholesterol absorption receptor (NPC1L1) was recently identified to be an important factor for HCV entry into host cells. Whether genetic variations of the NPC1L1 gene are associated with HCV infection is unknown.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom