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Volumn 12, Issue 2, 2001, Pages 85-90
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Homozygosity for the C677 → T mutation of 5,10-methylenetetrahydrofolate reductase and total plasma homocyst(e)ine are not associated with greater than normal risk of a first myocardial infarction in northern Sweden
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Author keywords
Homocysteine; Methylenetetrahydrofolate reductase gene; Myocardial infarction; Risk factors
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Indexed keywords
HOMOCYSTEINE;
METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);
OXIDOREDUCTASE;
ADULT;
ARTICLE;
CASE CONTROL STUDY;
CONTROLLED STUDY;
CORONARY RISK;
ENZYME BLOOD LEVEL;
FEMALE;
GENE MUTATION;
GENOTYPE;
HEART INFARCTION;
HOMOZYGOSITY;
HUMAN;
MAJOR CLINICAL STUDY;
MALE;
POINT MUTATION;
PRIORITY JOURNAL;
PROSPECTIVE STUDY;
REGRESSION ANALYSIS;
SWEDEN;
BLOOD;
GENETICS;
HOMOZYGOTE;
MIDDLE AGED;
PREVALENCE;
RISK FACTOR;
STATISTICAL MODEL;
CASE-CONTROL STUDIES;
FEMALE;
HOMOCYSTEINE;
HOMOZYGOTE;
HUMANS;
LOGISTIC MODELS;
MALE;
METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2);
MIDDLE AGED;
MYOCARDIAL INFARCTION;
OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS;
POINT MUTATION;
PREVALENCE;
PROSPECTIVE STUDIES;
RISK FACTORS;
SWEDEN;
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EID: 0034745480
PISSN: 09546928
EISSN: None
Source Type: Journal
DOI: 10.1097/00019501-200103000-00001 Document Type: Article |
Times cited : (21)
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References (35)
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