Frequency of Triple Mutations Involving Factor V, Prothrombin, and Methylenetetrahydrofolate Reductase Genes Among Patients Referred for Molecular Thrombophilia Workup in a Tertiary Care Center in Lebanon
Author:
Affiliation:
1. Department of Pathology and Laboratory Medicine, American University of Beirut Medical Center (AUBMC), Beirut, Lebanon.
2. Department of Internal Medicine, American University of Beirut Medical Center (AUBMC), Beirut, Lebanon.
Publisher
Mary Ann Liebert Inc
Subject
Genetics (clinical),General Medicine
Link
http://www.liebertpub.com/doi/pdf/10.1089/gtmb.2011.0114
Reference26 articles.
1. Association of deep venous thrombosis with prothrombotic gene polymorphism identified in lung cancer cases
2. 5, 10-Methylenetetrahydrofolate Reductase Gene Variants and Congenital Anomalies: A HuGE Review
3. The Prevalence of Methylenetetrahydrofolate Reductase 677 C-T, Factor V 1691 G-A, and Prothrombin 20210 G-A Mutations in Healthy Populations in Sétif, Algeria
4. A study on thrombophilic factors in Italian Behcet's patients
5. Coagulation factor V
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1. Prevalence of thrombophilia-associated mutations and their clinical significance in a large cohort of Lebanese patients;Meta Gene;2021-09
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3. Triple thrombophilic simultaneous mutations in patients after bariatric surgery: is there a role for screening in the Eastern Mediterranean?;Journal of Surgical Case Reports;2018-06-01
4. Comparison of the Performance of the CepheidXpert HemosILFactor II and Factor V and the ViennaLabFV-PTH-MTHFRStripAssay Kits for Molecular Thrombophilia Profiling;Genetic Testing and Molecular Biomarkers;2014-03
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