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Burden of rare exome sequence variants in PROC gene is associated with venous thromboembolism: a population-based study
BACKGROUND: Rare coding mutations underlying deficiencies of antithrombin and proteins C and S contribute to familial venous thromboembolism (VTE). It is uncertain whether rare variants play a role in the etiology of VTE in the general population. OBJECTIVES: We conducted a deep whole-exome sequenci...
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| Publicat a: | J Thromb Haemost |
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| Autors principals: | , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7787541/ https://ncbi.nlm.nih.gov/pubmed/31680443 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jth.14676 |
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