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Thromb Haemost 1998; 80(03): 519
DOI: 10.1055/s-0037-1615239
DOI: 10.1055/s-0037-1615239
Letters to the Editor
Hepatic Vein Thrombosis in a Patient with Mutant Prothrombin 20210A Allele
Further Information
Publication History
Received
18 March 1998
Accepted
02 April 1998
Publication Date:
08 December 2017 (online)
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References
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- 5 Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3’-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and increase in venous thrombosis. Blood 1996; 88: 3698-703.
- 6 Teofili L, De Stefano V, Leone G, Micalizzi P, Iovino MS, Alfano G, Bizzi B. Hematological causes of venous thrombosis in young people: high incidence of myeloproliferative disorder as underlying disease in patients with splanchnic venous thrombosis. Thromb Haemost 1992; 67: 297-301.
- 7 De Stefano V, Chiusolo P, Paciaroni K, Casorelli I, Rossi E, Molinari M, Servidei S, Tonali PA, Leone G. Prothrombin G20210A mutant genotype is a risk factor for cerebrovascular ischemic disease in young patients. Blood 1998; 91: 3562-5.
- 8 Bucciarelli P, Franchi F, Alatri A, Bettini P, Moia M. Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene. Thromb Haemost 1998; 79: 445-6.