无血栓栓塞事件的纯合子G20210A凝血酶原基因突变：病例报告 - Suppr | 超能文献

Homozygous G20210A prothrombin gene mutation without thromboembolic events: a case report.

作者信息

Alatri A, Franchi F, Moia M

出版信息

Thromb Haemost. 1998 Dec;80(6):1028-9.

Abstract

摘要

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Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review.凝血酶原G20210A基因突变所致复发性深静脉血栓形成和肺栓塞：病例报告及文献复习

J Investig Med High Impact Case Rep. 2022 Jan-Dec;10:23247096211058486. doi: 10.1177/23247096211058486.

2

Bilateral Superficial Femoral Artery Thrombosis in a 15-Year-Old Caucasian Male with Homozygous Prothrombin G20210A Genotype and Associated Antiphospholipid Syndrome.一名15岁白种男性，患有纯合子凝血酶原G20210A基因型及相关抗磷脂综合征，出现双侧股浅动脉血栓形成

Int J Angiol. 2016 Dec;25(5):e100-e105. doi: 10.1055/s-0035-1548557. Epub 2015 Mar 23.

3

Phenotypic Heterogeneity in Patients with Homozygous Prothrombin 20210AA Genotype. A paper from the 2005 William Beaumont Hospital Symposium on Molecular Pathology.纯合子凝血酶原20210AA基因型患者的表型异质性。一篇来自2005年威廉·博蒙特医院分子病理学研讨会的论文。

J Mol Diagn. 2006 Sep;8(4):420-5. doi: 10.2353/jmoldx.2006.060014.