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 | Zendy

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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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