Antithrombin gene mutation 5356–5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin α-helix D molecular pathology.
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| Title: | Antithrombin gene mutation 5356–5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin α-helix D molecular pathology. |
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| 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. Jul2005, Vol. 84 Issue 7, p485-486. 2p. |
| Database: | Academic Search Ultimate |
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