Identification of two point mutations associated with inherited antithrombin deficiency
Abstract Background Antithrombin (AT) is a serine protease inhibitor which exerts its anticoagulant effect through binding to serine residues in the active centers of procoagulant serine proteases. Its deficiency is associated with increased risk of venous thrombosis. We aim to investigate the patho...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMC
2024-12-01
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| Sarja: | Thrombosis Journal |
| Aiheet: | |
| Linkit: | https://doi.org/10.1186/s12959-024-00677-6 |
| Tagit: |
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