Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiency
Author:
Publisher
Springer Science and Business Media LLC
Link
https://link.springer.com/content/pdf/10.1007/s00277-023-05607-6.pdf
Reference25 articles.
1. Juhl D, Kuta P, Shneyder M et al (2021) Two novel variants in the protein S gene PROS1 are associated with protein S deficiency and thrombophilia. Acta Haematol 144(2):222–226. https://doi.org/10.1159/000508525
2. Ameku K, Higa M (2018) Rivaroxaban treatment for warfarin-refractory thrombosis in a patient with hereditary protein S deficiency. Case Rep Hematol 23(2018):5217301. https://doi.org/10.1155/2018/5217301
3. Miyata T, Maruyama K, Banno F et al (2016) Thrombophilia in East Asian countries: are there any genetic differences in these countries? Thromb J 14(Suppl 1):25. https://doi.org/10.1186/s12959-016-0109-x
4. Majumder R, Nguyen T (2021) Protein S: function, regulation, and clinical perspectives. Curr Opin Hematol 28(5):339–344. https://doi.org/10.1097/MOH.0000000000000663
5. Majid Z, Tahir F, Ahmed J et al (2020) Protein C deficiency as a risk factor for stroke in young adults: a review. Cureus 12(3):e7472. https://doi.org/10.7759/cureus.7472
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