The relationship of mutations in the MTHFR, prothrombin, and PAI-1 genes to plasma levels of homocysteine, prothrombin, and PAI-1 in children and adults

Thrombosis and Haemostasis

Volumn 81, Issue 5, 1999, Pages 739-744

  Balasa, Vinod V ^a   Gruppo, Ralph A ^a   Glueck, Charles J ^b   Stroop, Davis ^a   Becker, Ann ^a   Pillow, Ann ^a   Wang, Ping ^b  

^a CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^b JEWISH HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); HOMOCYSTEINE; PLASMINOGEN ACTIVATOR INHIBITOR 1; PROTHROMBIN;

ADOLESCENT; AGE; AMINO ACID BLOOD LEVEL; ARTICLE; CHILD; CONTROLLED STUDY; FEMALE; GENDER; GENE MUTATION; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MULTIPLE REGRESSION; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; RISK; THROMBOPHILIA; THROMBOSIS;

EID: 0032939953     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1614564     Document Type: Article

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