Does the MTHFR 677T allele alter the clinical phenotype in severe haemophilia A?
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference9 articles.
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2. Symptomatic onset of severe hemophilia A in childhood is dependent on the presence of prothrombotic risk factors;Escuriola Ettingshausen;Thromb. Haemost.,2001
3. Effect of the factor V Leiden mutation on the clinical expression of severe hemophilia A;Lee;Thromb. Haemost.,2000
4. Dacie JV, Lewis SM. Practical haematology. 9th ed. London: Harcourt Publishers Limited. p. 341–390.
5. A common genetic variation in the 3′ untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis;Poort;Blood,1996
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