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.
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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DbLabel: Academic Search Ultimate
An: 17252681
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  Data: 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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  Data: <searchLink fieldCode="JN" term="%22Annals+of+Hematology%22">Annals of Hematology</searchLink>. Jul2005, Vol. 84 Issue 7, p485-486. 2p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=17252681
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      – Type: doi
        Value: 10.1007/s00277-005-1045-1
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      – Code: eng
        Text: English
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        StartPage: 485
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      – TitleFull: 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.
        Type: main
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            NameFull: Steiner, M.
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            NameFull: Rolfs, A.
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            NameFull: Wangnick, M.
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            NameFull: Burstein, C.
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            NameFull: Freund, M.
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            – D: 01
              M: 07
              Text: Jul2005
              Type: published
              Y: 2005
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              Value: 84
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              Value: 7
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            – TitleFull: Annals of Hematology
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