Associated thrombophilic defects in essential thrombocythaemia: Their relationship with clinical manifestations
In order to assess the contribution of genetic and acquired thrombophilic defects in the risk of thrombosis in essential thrombocythaemia, we evaluated the prevalence of factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase C677T polymorphisms, homocysteinemia, protein C, prot...
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2004
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| Acceso en línea: | https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00493848_v112_n3_p131_Kornblihtt http://hdl.handle.net/20.500.12110/paper_00493848_v112_n3_p131_Kornblihtt |
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