A homozygosity state for 20210A prothrombin variant in a young woman as cause of a deep venous thrombosis during pregnancy [2]

European Journal of Haematology

Volumn 65, Issue 1, 2000, Pages 80-81

  Acquila, M ^a,b   Bicocchi, M P ^a   Mori, P G ^a   Odino, S ^a   Valetto, A ^a   Bottini, F ^a  

^a Haemophilia Laboratory   (Italy)

^b G GASLINI INSTITUTE   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

PROTHROMBIN;

ADULT; ANTICOAGULATION; CASE REPORT; DEEP VEIN THROMBOSIS; FEMALE; GENE MUTATION; HUMAN; LETTER; PREGNANCY COMPLICATION; PRIORITY JOURNAL;

3' UNTRANSLATED REGIONS; ADULT; EUROPEAN CONTINENTAL ANCESTRY GROUP; FACTOR V; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MALE; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); MIDDLE AGED; OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS; PREGNANCY; PREGNANCY COMPLICATIONS, HEMATOLOGIC; PROTHROMBIN; THROMBOPHILIA; THROMBOPHLEBITIS; VARIATION (GENETICS);

EID: 0033916971     PISSN: 09024441     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1600-0609.2000.9L140.x     Document Type: Letter

References (8)