3 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
| 1 | 34967380 | Rapid identification of a pathogenic variant of PROS1 in a thrombophilic family by whole exome sequencing: A case report. | 2021 Dec 30 | 1 |
| 2 | 32815916 | A case-report of two patients with hereditary protein S deficiency treated by rivaroxaban. | 2020 Sep | 1 |
| 3 | 24507871 | PROS1 mutations associated with protein S deficiency in Polish patients with residual vein obstruction on rivaroxaban therapy. | 2014 Jul | 1 |