TY  - GEN
AU  - Van Vlierberghe,H
AU  - Delanghe,J R
AU  - De Bie,S
AU  - Praet,M
AU  - De Paepe,A
AU  - Messiaen,L
AU  - De Vos,M
AU  - Leroux-Roels,G
TI  - Association between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis C
SN  - 0954-691X
PY  - 2001///1204
KW  - Adult
KW  - Aged
KW  - Alleles
KW  - Case-Control Studies
KW  - Chi-Square Distribution
KW  - Cohort Studies
KW  - Cysteine
KW  - genetics
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - epidemiology
KW  - Genetic Testing
KW  - Haptoglobins
KW  - analysis
KW  - Hepatitis C, Chronic
KW  - Humans
KW  - Male
KW  - Middle Aged
KW  - Mutation, Missense
KW  - Phenotype
KW  - Polymorphism, Genetic
KW  - Prevalence
KW  - Probability
KW  - Reference Values
KW  - Risk Assessment
KW  - Tyrosine
N1  - Publication Type: Comparative Study; Journal Article
UR  - https://doi.org/10.1097/00042737-200109000-00014
ER  -