Whole-exome sequencing in evaluation of patients with venous thromboembolism

Genetics play a significant role in venous thromboembolism (VTE), yet current clinical laboratory-based testing identifies a known heritable thrombophilia (factor V Leiden, prothrombin gene mutation G20210A, or a deficiency of protein C, protein S, or antithrombin) in only a minority of VTE patients...

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Bibliografske podrobnosti
izdano v:Blood Adv
Main Authors: Lee, Eun-Ju, Dykas, Daniel J., Leavitt, Andrew D., Camire, Rodney M., Ebberink, Eduard, García de Frutos, Pablo, Gnanasambandan, Kavitha, Gu, Sean X., Huntington, James A., Lentz, Steven R., Mertens, Koen, Parish, Christopher R., Rezaie, Alireza R., Sayeski, Peter P., Cromwell, Caroline, Bar, Noffar, Halene, Stephanie, Neparidze, Natalia, Parker, Terri L., Burns, Adrienne J., Dumont, Anne, Yao, Xiaopan, Chaar, Cassius Iyad Ochoa, Connors, Jean M., Bale, Allen E., Lee, Alfred Ian
Format: Artigo
Jezik:Inglês
Izdano: American Society of Hematology 2017
Teme:
Thrombosis and Hemostasis
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC5728544/
https://ncbi.nlm.nih.gov/pubmed/29296762
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2017005249
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