Antithrombin gene mutation 5356-5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin a-helix D molecular pathology.

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Bibliographic Details
Title: Antithrombin gene mutation 5356-5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin a-helix D molecular pathology.
Authors: Steiner, M.1 michael.steiner@med.uni-rostock.de, Steiner, B.2, Rolfs, A.3, Wangnick, M.1, Burstein, C.1, Freund, M.2, Schuff-Werner, P.1
Source: Annals of Hematology. Jan2005, Vol. 84 Issue 1, p56-58. 3p.
Database: Academic Search Ultimate
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