Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease

Thrombosis and Haemostasis

Volumn 83, Issue 1, 2000, Pages 20-22

  Renner, Wilfried ^a,b   Köppel, Herwig ^a   Brodmann, Marianne ^a   Pabst, Edmund ^a   Schallmoser, Katharina ^a   Toplak, Hermann ^a   Wascher, Thomas C ^a   Pilger, Ernst ^a  

^a UNIVERSITY OF GRAZ   (Austria)

^b MEDICAL UNIVERSITY OF GRAZ   (Austria)

Author keywords

Arteriosclerosis; Factor II; Factor V Leiden; Peripheral arterial occlusive disease; Prothrombin

Indexed keywords

BLOOD CLOTTING FACTOR 5; PROTHROMBIN;

ADULT; AGED; ARTICLE; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE MUTATION; HUMAN; MAJOR CLINICAL STUDY; MALE; PERIPHERAL OCCLUSIVE ARTERY DISEASE; PRIORITY JOURNAL;

EID: 0033979789     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1613750     Document Type: Article

References (25)

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