Van Vlierberghe, H <br/><br/>
Association between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis C.  [electronic resource] 

 -  European journal of gastroenterology & hepatology  Sep 2001 
 - 1077-81 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article 
<br/><br/><label>ISSN: </label>0954-691X 
<br/><br/><label>Standard No.: </label>10.1097/00042737-200109000-00014  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Alleles<br/>Case-Control Studies<br/>Chi-Square Distribution<br/>Cohort Studies<br/>Cysteine--genetics<br/>Female<br/>Genetic Predisposition to Disease--epidemiology<br/>Genetic Testing<br/>Haptoglobins--analysis<br/>Hepatitis C, Chronic--epidemiology<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation, Missense<br/>Phenotype<br/>Polymorphism, Genetic<br/>Prevalence<br/>Probability<br/>Reference Values<br/>Risk Assessment<br/>Tyrosine--genetics