Elevated total plasma homocysteine and 677C→T mutation of the 5,10- methylenetetrahydrofolate reductase gene in thrombotic vascular disease [5]

American Journal of Human Genetics

Volumn 59, Issue 1, 1996, Pages 262-264

  De Franchis, R ^a   Mancini, F P ^a   D'Angelo, A ^a   Sebastio, G ^a   Fermo, I ^a   De Stefano, V ^a   Margaglione, M ^a   Mazzola, G ^a   Di Minno, G ^a   Andria, G ^a  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); HOMOCYSTEINE;

ADULT; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENOTYPE; HOMOZYGOSITY; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; NUCLEIC ACID BASE SUBSTITUTION; PERIPHERAL OCCLUSIVE ARTERY DISEASE; PRIORITY JOURNAL; THROMBOSIS; VEIN OCCLUSION;

5,10-METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ADULT; FEMALE; GENE FREQUENCY; HOMOCYSTEINE; HOMOZYGOTE; HUMANS; ITALY; MALE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MIDDLE AGED; OXIDOREDUCTASES; POINT MUTATION; THROMBOSIS;

EID: 0029895024     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (0)