Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases. [electronic resource]
Producer: 19990528Description: 163-70 p. digitalISSN:- 0021-9150
- 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase -- genetics
- Age of Onset
- Coronary Disease -- blood
- Cystathionine beta-Synthase -- genetics
- Fasting
- Female
- Genotype
- Homocysteine -- blood
- Humans
- Hyperhomocysteinemia -- complications
- Male
- Methionine -- administration & dosage
- Methylenetetrahydrofolate Reductase (NADPH2)
- Oxidoreductases Acting on CH-NH Group Donors -- genetics
- Point Mutation
- Polymorphism, Genetic
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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