Human Genome Epidemiology Literature Finder
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Records 1 - 1 (of 1 Records) |
| Query Trace: Decision Making and SERPINC1[original query] |
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| Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease. Blood 2020 May . Desch Karl C, Ozel Ayse B, Halvorsen Matt, Jacobi Paula M, Golden Krista, Underwood Mary, Germain Marine, Tregouet David-Alexandre, Reitsma Pieter H, Kearon Clive, Mokry Lauren, Richards J Brent, Williams Frances, Li Jun Z, Goldstein David, Ginsburg Dav |
- Page last reviewed:Feb 1, 2024
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