Association Between the G20210A Polymorphism of Prothrombin Gene and Myocardial Infarction in Tunisian Population-Reference-Cited by-同舟云学术

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Association Between the G20210A Polymorphism of Prothrombin Gene and Myocardial Infarction in Tunisian Population

Published:2016-06-15 Issue:5 Volume:54 Page:653-664
ISSN:0006-2928
Container-title:Biochemical Genetics
language:en
Short-container-title:Biochem Genet

Author:

Kallel Amani,Sbaï Mohamed Hedi,Sédiri Yousra,Feki Moncef,Mourali Mohamed Sami,Mechmeche Rachid,Jemaa Riadh,Kaabachi Naziha

Funder

Ministry of Higher education of Tunisia

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine,Ecology, Evolution, Behavior and Systematics,Biochemistry

Link

http://link.springer.com/content/pdf/10.1007/s10528-016-9744-y.pdf

Reference48 articles.

1. Ajjan RA, Ariëns RAS (2009) Cardiovascular disease and heritability of the prothrombotic state. Blood Rev 23(2):67–68

2. Angchaisuksiri P, Pingsuthiwong V, Aryuchai K, Busabaranata M, Sura T, Atichartakarn V et al (2000) Prevalence of the G1691A prothrombin gene mutation in the Thai population. Am J Hematol 65(2):119–122

3. Anjana M, Subbock K, Nishat A, Gowhar S, Suvarna A, Jyothy A (2009) Prothrombin gene G20210A mutation is not a risk for ischemic stroke in a south Indian Hyderbadi population. Thromb Res 124(2):245–247

4. Arruda VR, Annichino-bizzacchi JM, Gonçalves MS, Costa FF (1997) Prevalence of prothrombin gene variant (G20210A) in venous thrombosis and arterial disease. Thrombosis haematosis 78(6):1430–1433

5. Berredjeb D, Fekih-Mrissa N, Haggui A, Nsiria B, Baraket N, Haouala H, Gritli N (2013) Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of myocardial infarction. Cardiovasc Pathol 22(1):39–41

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. ATR1 A1166C (rs5186), FII G20210A (rs1799963), FV G1691A (rs6025), FXIII 97G > T (rs11466016) and MTHFR A1298C (rs1801131) polymorphisms and the risk of ST-elevation myocardial infarction in young Mexican individuals;Molecular Biology Reports;2024-01-25

2. Factor V Leiden but not the factor II 20210G>A mutation is a risk factor for premature coronary artery disease: a case-control study in Iran;Research and Practice in Thrombosis and Haemostasis;2023-01

3. Genetic variations associated with coronary artery disease and myocardial infarction in the Arab world: a systematic review and meta-analysis;Highlights in BioScience;2020-07-22

4. Genetic polymorphisms of the hemostasis system;Yakut Medical Journal;2019

5. Mitochondrial Genome Mutations Associated with Myocardial Infarction;Disease Markers;2018

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