Absence of Factor V Leiden Mutation and Low Prothrombin G 20210 A Mutation Prevalence in a Healthy Moroccan Population

Florence Mathonnet; Sellama Nadifi; Valérie Serazin-Leroy; Mbarka Dakouane; Yves Giudicelli

doi:10.1055/s-0037-1613361

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Thromb Haemost 2002; 88(06): 1073-1074
DOI: 10.1055/s-0037-1613361

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Schattauer GmbH

Absence of Factor V Leiden Mutation and Low Prothrombin G 20210 A Mutation Prevalence in a Healthy Moroccan Population

Florence Mathonnet

¹Department of Biochemistry and Molecular Biology, Medical Faculty Paris-Ouest, University Paris V, CHI Poissy Cedex, France

,

Sellama Nadifi

²Laboratory of Human Genetics, Medical Faculty of Casablanca, University Hassan II, Morocco

,

Valérie Serazin-Leroy

¹Department of Biochemistry and Molecular Biology, Medical Faculty Paris-Ouest, University Paris V, CHI Poissy Cedex, France

,

Mbarka Dakouane

¹Department of Biochemistry and Molecular Biology, Medical Faculty Paris-Ouest, University Paris V, CHI Poissy Cedex, France

,

Yves Giudicelli

¹Department of Biochemistry and Molecular Biology, Medical Faculty Paris-Ouest, University Paris V, CHI Poissy Cedex, France

› Author Affiliations

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Publication History

Received 12 August 2002

Accepted after revision 12 September 2002

Publication Date:
09 December 2017 (online)

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References
1 Ridker PM, Hennekens CH, Lindpaintner K, Stampfer MJ, Eisenberg PR, Miletich JP. Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men. N Engl J Med 1995; 332: 912-7.

Crossref PubMed Search in Google Scholar
2 Poort SR, Rosendaal FR, Reitsma PH, Bertina RM. A common genetic variation in the 3' -untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996; 88: 3698-703.

PubMed Search in Google Scholar
3 Rees DC. The population genetics of factor V Leiden (Arg 506 Gin). Br J Haematol 1996; 95: 579-86.

Crossref PubMed Search in Google Scholar
4 Rees DC, Chapman NH, Webster MT, Guerreiro JF, Rochette J, Clegg JB. Born to clot: the European burden. Br J Haematol 1999; 105: 564-6.

Crossref PubMed Search in Google Scholar
5 Rees DC, Cox M, Clegg JB. World distribution of factor V Leiden. Lancet 1995; 346: 1133-4.

Crossref PubMed Search in Google Scholar
6 Gurgey A, Rustemov R, Parlak H, Balta G. Prevalence of factor V Leiden and Methylenetetrahydrofolate Reductase C677T mutations in Azerbaijan. Thromb Haemost 1998; 80: 520-1.

Thieme Connect PubMed Search in Google Scholar
7 Togrul J, Rustemov R, Gurgey A, Altay S, Altay C. Prevalence of the prothrombin gene G20210A mutation in Azerbaijan. Br J Haematol 2000; 108: 887-8.

Crossref PubMed Search in Google Scholar
8 Gurgey A, Kudayarov DK, Tuncer M, Parlak H, Altay C. The factor V Leiden and prothrombin G20210A mutations in Kirghiz population. Thromb Haemost 2000; 84: 356.

Thieme Connect PubMed Search in Google Scholar
9 Ozbek U, Tangiin Y. Frequency of factor V Leiden (Arg506Gln) in Turkey. Br J Haematol 1997; 97: 504-5.

Crossref PubMed Search in Google Scholar
10 Gurgey A, Hicsomnez G, Parlak H, Balta G, Celiker A. The prothrombin gene 20210 G-A mutation in Turkish patients with thrombosis. Am J Hematol 1999; 59: 179-80.

PubMed Search in Google Scholar
11 Seligsohn U, Zivelin A. Thrombophilia as a multigenic disorder. Thromb Haemost 1997; 78 (01) 297-301.

Thieme Connect PubMed Search in Google Scholar
12 Awidi A, Shannak M, Bseiso A, Kailani MAM, Kailani MA, Omar N, Anshasi B, Sakarneh N. High prevalence of factor V Leiden in healthy Jordanian arabs. Thromb Haemost 1999; 81: 582-4.

Thieme Connect PubMed Search in Google Scholar
13 Rosen E, Renbaum P, Heyd J, Levy-Lahad E. High frequency of factor V Leiden in a population of Israeli Arabs. Thromb Haemost 1999; 82 (06) 1768.

Thieme Connect PubMed Search in Google Scholar
14 Dzimiri N, Meyer B. World distribution of factor V Leiden. Lancet 1996; 347: 481-2.

PubMed Search in Google Scholar
15 Hammoud DF, Eldibanny MM, Nowak JA. Prevalence of the factor V Leiden mutation in the Egyptian population. (Abstract). Blood 1996; 88 (10) (Suppl. 01) 73b.

PubMed Search in Google Scholar
16 Chafa O, Reghis A, Aubert A, Fischer AM. Prevalence of the FVQ506 (factor V Leiden) mutation in the normal and thrombophilic Algerian population. Br J Haematol 1997; 97: 688-9.

PubMed Search in Google Scholar
17 Helley D, Chafa O, Yaker NJ, Reghis A, Fischer AM. Prevalence of the prothrombin gene 20210A mutation in thrombophilic and healthy Algerian subjects. Thromb Haemost 1999; 82: 1554-5.

Thieme Connect PubMed Search in Google Scholar
18 Gandrille S, Alhenc-Gelas M, Aiach M. A rapid screening method for the factor V Arg 506 Gin mutation. Blood Coag Fibrinol 1995; 06: 245-9.

Crossref PubMed Search in Google Scholar
19 Alhenc-Gelas M, Arnaud E, Nicaud V, Aubry ML, Fiessinger JN, Aiach M, Emmerich J. Venous thromboembolic disease and the prothrombin methylene tetrahydrofolate reductase and factor V genes. Thromb Haemost 1999; 81: 506-10.

Thieme Connect PubMed Search in Google Scholar
20 Zivelin A, Griffin JH, Xu X, Pabinger I, Samama M, Conard J, Brenner B, Eldor A, Seligsohn U. A single genetic origin for a common Caucasian risk factor for venous thrombosis. Blood 1997; 02: 397-402.

PubMed Search in Google Scholar
21 Rosendaal FR, Doggen CJ, Zivelin A, Arruda VR, Aiach M, Siscovick DS, Hillarp A, Watzke HH, Bernardi F, Cumming AM, Preston FE, Reitsma PH. Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost 1998; 79: 706-8.

Thieme Connect PubMed Search in Google Scholar
22 Zheng H, Tzeng CC, Butt C, Randell E, Xie YG. An extremely low prevalence of factor V Leiden, FIIG20210A and FXIIIV34L in Taiwan Chinese population. Thromb Haemost 2002; 87: 1081-2.

Thieme Connect PubMed Search in Google Scholar
23 Dilley A, Austin H, Hooper WC, El-Jamil M, Whitsett C, Wenger NK, Benson J, Evatt B. Prevalence of the prothrombin 20210 G-to-A variant in blacks: infants, patients with venous thrombosis, patients with myocardial infarction, and control subjects. J Lab Clin Med 1998; 132: 452-5.

Crossref PubMed Search in Google Scholar

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Absence of Factor V Leiden Mutation and Low Prothrombin G 20210 A Mutation Prevalence in a Healthy Moroccan Population

Publication History

References