Prevalence of the factor II G20210A mutation in symptomatic patients with inherited thrombophilia [1]

Thrombosis and Haemostasis

Volumn 80, Issue 2, 1998, Pages 342-343

  De Stefano, V ^a   Chiusolo, P ^a   Paciaroni, K ^a   Casorelli, I ^a   Di Mario, A ^a   Rossi, E ^a   Leone, G ^a  

^a CATHOLIC UNIVERSITY   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 5; PROTHROMBIN;

ALLELE; CONTROLLED STUDY; GENE FREQUENCY; GENE MUTATION; HETEROZYGOTE; HUMAN; LETTER; MAJOR CLINICAL STUDY; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL; RISK FACTOR; THROMBOPHILIA; VEIN THROMBOSIS;

EID: 0031825902     PISSN: 03406245     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-0037-1615199     Document Type: Letter

References (3)