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thrombophilia due to antithrombin iii deficiency
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SERPINC1
Hereditary antithrombin III deficiency: biochemical aspects
Antithrombin III mutation database: first update. For the Thrombin and its Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis
A recurrent deletion in the antithrombin gene, AT106-108(-6 bp), identified by DNA heteroduplex detection
A common point mutation producing type 1A antithrombin III deficiency: AT129 CGA to TGA (Arg to Stop)
Molecular basis of inherited human antithrombin deficiency
Structural basis of latency in plasminogen activator inhibitor-1
Commercial antithrombin concentrate contains inactive L-forms of antithrombin
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