APA (7th ed.) Citation

F, X., X, C., Q, X., A, Z., X, L., M, W., . . . H, X. (2026). SERPINC1 mutations and thrombotic events in inherited antithrombin deficiency: A study on the han population of East China. Orphanet journal of rare diseases, 21(1), . https://doi.org/10.1186/s13023-026-04200-0

Chicago Style (17th ed.) Citation

F, Xu, Chen X, Xu Q, Zou A, Li X, Wang M, Yang L, and Xie H. "SERPINC1 Mutations and Thrombotic Events in Inherited Antithrombin Deficiency: A Study on the Han Population of East China." Orphanet Journal of Rare Diseases 21, no. 1 (2026). https://doi.org/10.1186/s13023-026-04200-0.

MLA (9th ed.) Citation

F, Xu, et al. "SERPINC1 Mutations and Thrombotic Events in Inherited Antithrombin Deficiency: A Study on the Han Population of East China." Orphanet Journal of Rare Diseases, vol. 21, no. 1, 2026, https://doi.org/10.1186/s13023-026-04200-0.