APA (7th ed.) Citation

Steiner, M., Steiner, B., Rolfs, A., Wangnick, M., Burstein, C., Freund, M., & Schuff-Werner, P. (2005). Antithrombin gene mutation 5356–5364*delCTT with type I deficiency and early-onset thrombophilia and a brief review of the antithrombin α-helix D molecular pathology. Annals of Hematology, 84(7), 485. https://doi.org/10.1007/s00277-005-1045-1

Chicago Style (17th ed.) Citation

Steiner, M., B. Steiner, A. Rolfs, M. Wangnick, C. Burstein, M. Freund, and P. Schuff-Werner. "Antithrombin Gene Mutation 5356–5364*delCTT with Type I Deficiency and Early-onset Thrombophilia and a Brief Review of the Antithrombin α-helix D Molecular Pathology." Annals of Hematology 84, no. 7 (2005): 485. https://doi.org/10.1007/s00277-005-1045-1.

MLA (9th ed.) Citation

Steiner, M., et al. "Antithrombin Gene Mutation 5356–5364*delCTT with Type I Deficiency and Early-onset Thrombophilia and a Brief Review of the Antithrombin α-helix D Molecular Pathology." Annals of Hematology, vol. 84, no. 7, 2005, p. 485, https://doi.org/10.1007/s00277-005-1045-1.