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凝血酶原20210A突变及其临床意义 被引量:3

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摘要 遗传流行病学资料显示,血栓形成患者中60%具有家族性[1].目前,可致高凝状态和静脉血栓形成的遗传缺陷中最普遍的是蛋白G、蛋白S、抗疑血酶Ⅲ和属于因子V Leiden突变的抗活化蛋白C等缺陷.新近,凝血酶原20210A突变被认为是又一种致血栓形成的遗传缺陷[2].现就凝血酶原20210A突变及其临床意义作一综述.
出处 《血栓与止血学》 2003年第2期86-88,共3页 Chinese Journal of Thrombosis and Hemostasis
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