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DOI: GENETIC RISK FACTORS ASSOCIATED WITH THROMBOSIS IN A SAMPLE OF IRAQ POPULATION
Muhanad S Ramadhan , Department of Medical Biotechnology, College of Biotechnology, Al-Nahrain University, Baghdad, IraqAbstract
Thrombosis is a complex disorder influenced by various genetic factors. This research paper aims to investigate the genetic risk factors associated with thrombosis in a sample of the Iraq population. Understanding the genetic determinants of thrombosis is crucial for early detection, prevention, and personalized treatment strategies. This study examines a sample of the Iraq population to identify specific genetic variations and polymorphisms that may contribute to an increased risk of thrombosis. Through genetic analysis techniques, such as polymerase chain reaction (PCR) and sequencing, the study explores the prevalence and potential impact of these genetic risk factors on thrombosis. The findings provide valuable insights into the genetic underpinnings of thrombosis in the Iraq population and may have implications for risk assessment, diagnosis, and targeted interventions.
Keywords
Genetic risk factors, Thrombosis, Iraq population
References
Ali N, Hedyeh F T, Mohammad N, Sadaf T,Maryam J H, Fahimeh S T and Seyed R S(2013), “Screening for mutations in 10 exonsof the coagulation factor gene”, EuropeanJ.biology., Vol. 3, No. 3, pp. 589-592.
Asselta R and Peyvandi F (2009), Factor Vdeficiency SeminThrombHemost ., Vol. 35,No. 4, pp. 382-9.
Asselta R, Tenchini M L and Duga S (2006),“Inherited defects of coagulation factor V: thehemorrhagic side”, J.ThrombHaemost., Vol.4, No. 1, pp. 26-34.
Castoldi E, Simioni P, Kalafatis M, LunghiB, Tormene D, Girelli D, Girolami Aand Bernardi F (2000), “The prothrom-binase complex in a thrombophilic family”,Blood, Vol. 15, No. 4, pp. 1443-8.
Freeman W and Company H (2000).,Genetic Analysis, ISBN., 978(1):4180-5357.
Greer I A (2003), Best Pract Res Clin ObstetGynaecol., Vol. 17, No. 3, pp. 413-25.
7. Huang D D, Wang X F and Chen H Y (2010),“Analysis of phenotype and genotype in fourChinese pedigrees with inheritedcoagulation factor V deficiency”,ZhonghuaXue YeXueZaZhi, Vol. 31, p. 149.
Kumar and Vinay (2007), Robbins BasicPathology, Philadelphia: Saunders/Elsevier.ISBN: 978(1):4160-2973.
9. Lewis R (2004), Human Genetics:Concepts and Applications, 6th ed., McGrawHill. ISBN., 0072951745.
10. Ossowski S, Schneeberger K and Lucas-Lledó J I (2010), “The rate and molecularspectrum of spontaneous mutations”,Science., Vol. 1, No. 5961, pp. 92-4.
11. Press R D, Bauer K A, Kujovich J L, Heit J A(2002), Arch Pathol Lab Med., Vol. 126, No.11, pp. 1304-18.
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