Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease
| Autor: | Desch, Karl C. 1, 1, Ozel, Ayse B. 2, Halvorsen, Matt 3, Jacobi, Paula M. 1, Golden, Krista 1, Underwood, Mary 1, Germain, Marine 4, Tregouet, David-Alexandre 4, Reitsma, Pieter H. 5, Kearon, Clive 6, Mokry, Lauren 7, Richards, J. Brent 7, Williams, Frances 8, Li, Jun Z. 2, Goldstein, David 9, Ginsburg, David 1, 2, 10 |
|---|---|
| Zdroj: | In Blood 30 July 2020 136(5):533-541 |
| Databáze: | ScienceDirect |
| Externí odkaz: |
|