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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Blood Adv
मुख्य लेखकों: 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
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: American Society of Hematology 2017
विषय:
Thrombosis and Hemostasis
ऑनलाइन पहुंच: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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