Associated Papers
Clinical and genetic characterization of a protein S deficient patient with multiple thrombotic events.
Chen Y et al.
International Journal of Laboratory Hematology, 2024
Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiency.
Xu F et al.
Annals of Hematology, 2024
Case Report: PROS1 (c.76+2_76+3del) pathogenic mutation causes pulmonary embolism.
Ding P et al.
Frontiers in Cardiovascular Medicine, 2024
Molecular profiling of TAM tyrosine kinase receptors and ligands in endometrial carcinoma: An in silico-study.
Dilara Fatma Akin et al.
Taiwanese Journal of Obstetrics & Gynecology, 2023
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