Family history, plasma homocysteine, and age at onset of symptoms of myocardial ischemia in patients with different methylenetetrahydrofolate reductase genotypes

American Journal of Cardiology

Volumn 95, Issue 12, 2005, Pages 1420-1424

  Mager, Aviv ^a   Koren Morag, Nira ^b   Shohat, Mordechai ^b   Harell, Daniella ^b   Battler, Alexander ^b  

^a RABIN MEDICAL CENTER   (Israel)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); HOMOCYSTEINE;

ADULT; ARTICLE; CONTROLLED STUDY; CORONARY ARTERY DISEASE; DISEASE ASSOCIATION; FAMILY HISTORY; FEMALE; GENE MUTATION; GENOTYPE; HEART MUSCLE ISCHEMIA; HOMOZYGOTE; HUMAN; MAJOR CLINICAL STUDY; MALE; MULTIPLE REGRESSION; ONSET AGE; PRIORITY JOURNAL; RISK FACTOR; SCREENING; SMOKING; SYMPTOM;

AGE OF ONSET; AGED; DNA; ELECTROPHORESIS, AGAR GEL; FEMALE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HOMOCYSTEINE; HUMANS; HYPERHOMOCYSTEINEMIA; ISRAEL; MALE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MUTATION; MYOCARDIAL ISCHEMIA; PEDIGREE; POLYMERASE CHAIN REACTION; REGRESSION ANALYSIS; RISK FACTORS; SMOKING;

EID: 20444478969     PISSN: 00029149     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.amjcard.2005.01.097     Document Type: Article

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