Prothrombin G20210A Mutation is Rare but not Absent Among North Indian Patients with Thromboembolic Events-Reference-Cited by-同舟云学术

Prothrombin G20210A Mutation is Rare but not Absent Among North Indian Patients with Thromboembolic Events

Published:2024-03-25 Issue:3 Volume:40 Page:522-526
ISSN:0971-4502
Container-title:Indian Journal of Hematology and Blood Transfusion
language:en
Short-container-title:Indian J Hematol Blood Transfus

Author:

Satyarthi Priti,Ray Debadrita,Kumar Vasant,Hans Chander,Senee Hari Kishan,Ahluwalia Jasmina,Das Reena,Jain Arihant,Mahesh Kartik Vinay,Kumar Narender^ORCID

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s12288-024-01741-x.pdf

Reference16 articles.

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2. Stevens SM, Woller SC, Bauer KA, Kasthuri R, Cushman M, Streiff M et al (2016) Guidance for the evaluation and treatment of hereditary and acquired thrombophilia. J Thromb Thrombolysis 41:154–164. https://doi.org/10.1007/s11239-015-1316-1

3. Rosendaal FR, Doggen CJ, Zivelin A, Arruda VR, Aiach M, Siscovick DS et al (1998) Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost 79:706–708

4. Poort SR, Rosendaal FR, Reitsma PH, Bertina RM (1996) 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 88:3698–3703

5. Shafia S, Zargar MH, Khan N, Ahmad R, Shah ZA, Asimi R (2018) High prevalence of factor V Leiden and prothrombin G20101A mutations in Kashmiri patients with venous thromboembolism. Gene 654:1–9. https://doi.org/10.1016/J.GENE.2018.02.031