MM, B., S, A., H, H., & S, S. (2026). Identification of novel PROS1 variants through systematic analysis of patients with suspected hereditary protein S deficiency. Research and practice in thrombosis and haemostasis, 10(3), 103432. https://doi.org/10.1016/j.rpth.2026.103432
Chicago Style (17th ed.) CitationMM, Bartylla, Achenbach S, Hackstein H, and Schneider S. "Identification of Novel PROS1 Variants Through Systematic Analysis of Patients with Suspected Hereditary Protein S Deficiency." Research and Practice in Thrombosis and Haemostasis 10, no. 3 (2026): 103432. https://doi.org/10.1016/j.rpth.2026.103432.
MLA (9th ed.) CitationMM, Bartylla, et al. "Identification of Novel PROS1 Variants Through Systematic Analysis of Patients with Suspected Hereditary Protein S Deficiency." Research and Practice in Thrombosis and Haemostasis, vol. 10, no. 3, 2026, p. 103432, https://doi.org/10.1016/j.rpth.2026.103432.