一名凝血酶原基因G20210A突变杂合子患者的布加综合征 - Suppr

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Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.

作者信息

Bucciarelli P, Franchi F, Alatri A, Bettini P, Moia M

出版信息

Thromb Haemost. 1998 Feb;79(2):445-6.

PMID:9493607

Abstract

摘要

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Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene.一名凝血酶原基因G20210A突变杂合子患者的布加综合征

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A Novel Culprit in a Patient with Budd-Chiari Syndrome.布加综合征患者的一个新病因

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Risk of Budd-Chiari syndrome associated with factor V Leiden and G20210A prothrombin mutation: a meta-analysis.风险与因子 V 莱顿和 G20210A 凝血酶原突变相关的布加氏综合征：荟萃分析。

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Concomitant homozygosity for the prothrombin gene variant with mild deficiency of antithrombin III in a patient with multiple hepatic infarctions: a case report.一名患有多发性肝梗死患者同时存在凝血酶原基因变异纯合子和抗凝血酶III轻度缺乏：病例报告

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