Association between Cys282Tyr missense mutation and haptoglobin phenotype polymorphism in patients with chronic hepatitis C. [electronic resource]
Producer: 20011204Description: 1077-81 p. digitalISSN:- 0954-691X
- Adult
- Aged
- Alleles
- Case-Control Studies
- Chi-Square Distribution
- Cohort Studies
- Cysteine -- genetics
- Female
- Genetic Predisposition to Disease -- epidemiology
- Genetic Testing
- Haptoglobins -- analysis
- Hepatitis C, Chronic -- epidemiology
- Humans
- Male
- Middle Aged
- Mutation, Missense
- Phenotype
- Polymorphism, Genetic
- Prevalence
- Probability
- Reference Values
- Risk Assessment
- Tyrosine -- genetics
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Publication Type: Comparative Study; Journal Article
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