A heparin cofactor II mutation (HCII Rimini) combined with factor V Leiden or type I protein C deficiency in two unrelated thrombophilic subjects

Thrombosis and Haemostasis

Volumn 76, Issue 4, 1996, Pages 505-509

  Bernardi, F ^a   Legnani, C ^b   Micheletti, F ^a   Lunghi, B ^a   Ferraresi, P ^a   Palareti, G ^b   Biagi, R ^a   Marchetti, G ^a  

^a UNIVERSITY OF FERRARA   (Italy)

^b UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ANTITHROMBIN III; HEPARIN COFACTOR II;

ADULT; ARTICLE; BLOOD CLOTTING FACTOR 5 DEFICIENCY; CASE REPORT; GENE MUTATION; HETEROZYGOSITY; HUMAN; PEDIGREE; PRIORITY JOURNAL; PROTEIN C DEFICIENCY; THROMBOPHILIA;

EID: 0029806282     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0038-1650612     Document Type: Article

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