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.
Saved in:
| 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. |
|---|---|
| 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 |
| ISSN: | 09395555 |
|---|---|
| DOI: | 10.1007/s00277-005-1045-1 |
