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Information Journal Paper

Title

Prevalence of the prothrombin G20210A mutation among ischemic stroke patients

Pages

  234-237

Abstract

 Introduction: Ischemic stroke is characterized as a sudden neurological deficit attributed to an acute focal injury of the central nervous system by a vascular cause. This study was performed to determine the frequency of G20210A mutation in the prothrombin gene and its effectiveness on the incidence of ischemic stroke in the Erbil city of Kurdistan region, Iraq. Methods: A total of 50 patients with ischemic stroke was analyzed for the detection of prothrombin gene mutation (G20210A), using polymerase chain reaction (PCR), Restriction fragment length polymorphism (RFLP) with Hind III restriction enzyme. Results: We observed no evidence of an association between ischemic stroke and G20210A mutation in the prothrombin gene in this region. Conclusion: Our finding demonstrates that prothrombotic gene variant seems not to be linked to the incidence of ischemic stroke in Erbil region.

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    APA: Copy

    Ahmed, Salar A., Hameed, Sazgar A., Hussen, Bashdar M., & Salihi, Abbas. (2020). Prevalence of the prothrombin G20210A mutation among ischemic stroke patients. JOURNAL OF CARDIOVASCULAR AND THORACIC RESEARCH, 12(3), 234-237. SID. https://sid.ir/paper/768682/en

    Vancouver: Copy

    Ahmed Salar A., Hameed Sazgar A., Hussen Bashdar M., Salihi Abbas. Prevalence of the prothrombin G20210A mutation among ischemic stroke patients. JOURNAL OF CARDIOVASCULAR AND THORACIC RESEARCH[Internet]. 2020;12(3):234-237. Available from: https://sid.ir/paper/768682/en

    IEEE: Copy

    Salar A. Ahmed, Sazgar A. Hameed, Bashdar M. Hussen, and Abbas Salihi, “Prevalence of the prothrombin G20210A mutation among ischemic stroke patients,” JOURNAL OF CARDIOVASCULAR AND THORACIC RESEARCH, vol. 12, no. 3, pp. 234–237, 2020, [Online]. Available: https://sid.ir/paper/768682/en

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