HuGE Literature Finder
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Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease. Blood 2020 May . Desch Karl, Ozel Ayse Bilge, Halvorsen Matt, Jacobi Paula M, Golden Krista L, Underwood Mary I, Germain Marine, Trégouët David-Alexandre, Reitsma Pieter H, Kearon Clive, Mokry Lauren, Richards Brent, Williams Frances, Li Jun, Goldstein David B, Ginsburg Dav |
- Page last reviewed:Oct 1, 2021
- Page last updated:May 18, 2022
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