Methylenetetrahydrofolate reductase (MTHFR) mutation, homocyst(e)ine, and coronary artery disease [7] (multiple letters)

Circulation

Volumn 96, Issue 8, 1997, Pages 2738-2740

  Wilcken, D E L ^a   Xing Li Wang, ^a   Wilcken, B ^a   Ma, J ^a   Hennekens, C H ^a   Stampfer, M ^a  

^a UNIVERSITY OF NEW SOUTH WALES   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); FOLIC ACID; HOMOCYSTEINE;

BODY MASS; CARDIOVASCULAR RISK; CORONARY ARTERY DISEASE; DISEASE PREDISPOSITION; GENE MUTATION; GENOTYPE; HEART INFARCTION; HOMOCYSTINURIA; HOMOZYGOSITY; INBORN ERROR OF METABOLISM; LETTER; PRIORITY JOURNAL; RISK FACTOR;

ADULT; CORONARY DISEASE; HOMOCYSTEINE; HOMOCYSTINE; HUMANS; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MIDDLE AGED; MUTATION; OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS; PROSPECTIVE STUDIES;

EID: 0030845376     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)