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The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families.

作者信息

Zoller B, Svensson P J, Dahlback B, Hillarp A

出版信息

Blood. 1998 Mar 15;91(6):2210-1.

PMID:9490712
Abstract
摘要

相似文献

1
The A20210 allele of the prothrombin gene is frequently associated with the factor V Arg 506 to Gln mutation but not with protein S deficiency in thrombophilic families.凝血酶原基因的A20210等位基因在血栓形成倾向家族中常与因子V精氨酸506突变为谷氨酰胺相关，但与蛋白S缺乏无关。
Blood. 1998 Mar 15;91(6):2210-1.
2
The prothrombin 20210 A allele is frequently coinherited in young carriers of the factor V Arg 506 to Gln mutation with venous thrombophilia.凝血酶原20210 A等位基因在因子V Arg 506至Gln突变且患有静脉血栓形成倾向的年轻携带者中经常共同遗传。
Blood. 1998 Mar 15;91(6):2209-10.
3
The A20210 allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic families.凝血酶原基因的A20210等位基因在血栓形成倾向家族中并不常与因子V Arg 506至Gln突变相关。
Blood. 1997 Aug 15;90(4):1711.
4
Rapid simultaneous screening of factor V Leiden and G20210A prothrombin variant by multiplex polymerase chain reaction on whole blood.
Blood. 1998 Mar 15;91(6):2208-9.
5
Inherited thrombophilia and first venous thromboembolism during pregnancy and puerperium.遗传性血栓形成倾向与妊娠和产褥期首次静脉血栓栓塞症
Thromb Haemost. 2002 May;87(5):791-5.
6
Pregnancy-related recurrent events in thrombophilic women with previous venous thromboembolism.既往有静脉血栓栓塞史的易栓症女性的妊娠相关复发性事件。
Thromb Haemost. 2001 Sep;86(3):929.
7
Contribution of prothrombin 20210A allele and factor V Leiden mutation to thrombosis risk in thrombophilic families with other hemostatic deficiencies.凝血酶原20210A等位基因和因子V莱顿突变对伴有其他止血缺陷的易栓症家族血栓形成风险的影响。
Haematologica. 2001 Nov;86(11):1200-8.
8
Genetic Risk Factors in Venous Thromboembolism.静脉血栓栓塞症的遗传风险因素
Adv Exp Med Biol. 2017;906:253-272. doi: 10.1007/5584_2016_120.
9
The utility of thrombophilia testing.血栓形成倾向检测的效用。
Clin Chem Lab Med. 2014 Apr;52(4):495-7. doi: 10.1515/cclm-2013-0559.
10
Thrombophilia in childhood: to test or not to test.儿童期血栓形成倾向：检测还是不检测。
Semin Thromb Hemost. 2011 Oct;37(7):794-801. doi: 10.1055/s-0031-1297170. Epub 2011 Dec 20.

引用本文的文献

1
Thrombosis risk in single- and double-heterozygous carriers of factor V Leiden and prothrombin G20210A in FinnGen and the UK Biobank.在 FinnGen 和 UK Biobank 中，单一和双重杂合子携带因子 V Leiden 和凝血酶原 G20210A 的血栓形成风险。
Blood. 2024 Jun 6;143(23):2425-2432. doi: 10.1182/blood.2023023326.
2
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.
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.
4
Congenital thrombophilia and thrombosis: a study in a single centre.先天性血栓形成倾向与血栓形成：单中心研究
Arch Dis Child. 1999 Aug;81(2):176-8. doi: 10.1136/adc.81.2.176.