APA (7th ed.) Citation

Ruf, M., Cunningham, S., Wandersee, A., Brox, R., Achenbach, S., Strobel, J., . . . Schneider, S. (2024). SERPINC1 c.1247dupC: A novel SERPINC1 gene mutation associated with familial thrombosis results in a secretion defect and quantitative antithrombin deficiency. Thrombosis Journal, 22(1), 1. https://doi.org/10.1186/s12959-024-00589-5

Chicago Style (17th ed.) Citation

Ruf, Maximilian, Sarah Cunningham, Alexandra Wandersee, Regine Brox, Susanne Achenbach, Julian Strobel, Holger Hackstein, and Sabine Schneider. "SERPINC1 C.1247dupC: A Novel SERPINC1 Gene Mutation Associated with Familial Thrombosis Results in a Secretion Defect and Quantitative Antithrombin Deficiency." Thrombosis Journal 22, no. 1 (2024): 1. https://doi.org/10.1186/s12959-024-00589-5.

MLA (9th ed.) Citation

Ruf, Maximilian, et al. "SERPINC1 C.1247dupC: A Novel SERPINC1 Gene Mutation Associated with Familial Thrombosis Results in a Secretion Defect and Quantitative Antithrombin Deficiency." Thrombosis Journal, vol. 22, no. 1, 2024, p. 1, https://doi.org/10.1186/s12959-024-00589-5.