Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease. [electronic resource]
Producer: 19960221Description: 35-41 p. digitalISSN:- 0002-9297
- Alleles
- Amino Acid Metabolism, Inborn Errors -- enzymology
- Base Sequence
- Cardiovascular Diseases -- enzymology
- Confidence Intervals
- Cystathionine beta-Synthase -- genetics
- DNA Primers
- Genotype
- Homocysteine -- blood
- Humans
- Methylenetetrahydrofolate Reductase (NADPH2)
- Molecular Sequence Data
- Oxidoreductases Acting on CH-NH Group Donors -- biosynthesis
- Point Mutation
- Polymerase Chain Reaction
- Prevalence
- Reference Values
- Risk Factors
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Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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