The frequency of Factor V 1691G-A mutation in Iraqi Turks

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The frequency of Factor V G1691A (Leiden) mutation in Iraqi Turks.

Factor V Leiden (FVL) mutation (G1691A) is a risk factor for the development of venous thromboembolic disorders. Hereditary disorders that predispose to thrombosis include antithrombin, protein C, and protein S deficiency, as well as such hereditary defects as Factor V G1691A (Leiden) (FVL) and prothrombin G20210A mutation [1,2]. FVL causes activated protein C resistance and is the most common ...

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ژورنال

عنوان ژورنال: Turkish Journal of Hematology

سال: 2011

ISSN: 1300-7777,1308-5263

DOI: 10.5152/tjh.2011.46