Identification of novel PROS1 variants through systematic analysis of patients with suspected hereditary protein S deficiency.
Saved in:
| Title: | Identification of novel PROS1 variants through systematic analysis of patients with suspected hereditary protein S deficiency. |
|---|---|
| Authors: | Bartylla MM; Department of Transfusion Medicine and Hemostaseology, Friedrich-Alexander University Erlangen-Nuremberg, University Hospital Erlangen, Erlangen, Germany., Achenbach S; Department of Transfusion Medicine and Hemostaseology, Friedrich-Alexander University Erlangen-Nuremberg, University Hospital Erlangen, Erlangen, Germany., Hackstein H; Department of Transfusion Medicine and Hemostaseology, Friedrich-Alexander University Erlangen-Nuremberg, University Hospital Erlangen, Erlangen, Germany., Schneider S; Department of Transfusion Medicine and Hemostaseology, Friedrich-Alexander University Erlangen-Nuremberg, University Hospital Erlangen, Erlangen, Germany. |
| Source: | Research and practice in thrombosis and haemostasis [Res Pract Thromb Haemost] 2026 Mar 25; Vol. 10 (3), pp. 103432. Date of Electronic Publication: 2026 Mar 25 (Print Publication: 2026). |
| Publication Type: | Journal Article |
| Journal Info: | Publisher: Elsevier Country of Publication: United States NLM ID: 101703775 Publication Model: eCollection Cited Medium: Internet ISSN: 2475-0379 (Electronic) Linking ISSN: 24750379 NLM ISO Abbreviation: Res Pract Thromb Haemost Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
Be the first to leave a comment!