Variants in FIX propeptide associated with vitamin K antagonist hypersensitivity: functional analysis and additional data confirming the common founder mutations.

MLA

Pezeshkpoor, Behnaz, et al. “Variants in FIX Propeptide Associated with Vitamin K Antagonist Hypersensitivity: Functional Analysis and Additional Data Confirming the Common Founder Mutations.” Annals of Hematology, vol. 97, no. 6, June 2018, pp. 1061–69. EBSCOhost, https://doi.org/10.1007/s00277-018-3264-2.

APA

Pezeshkpoor, B., Czogalla, K. J., Caspers, M., Berkemeier, A.-C., Liphardt, K., Ghosh, S., Kellner, M., Ulrich, S., Pavlova, A., & Oldenburg, J. (2018). Variants in FIX propeptide associated with vitamin K antagonist hypersensitivity: functional analysis and additional data confirming the common founder mutations. Annals of Hematology, 97(6), 1061–1069. https://doi.org/10.1007/s00277-018-3264-2

Chicago

Pezeshkpoor, Behnaz, Katrin J. Czogalla, Michael Caspers, Ann-Cristin Berkemeier, Kerstin Liphardt, Suvoshree Ghosh, Marco Kellner, Silvia Ulrich, Anna Pavlova, and Johannes Oldenburg. 2018. “Variants in FIX Propeptide Associated with Vitamin K Antagonist Hypersensitivity: Functional Analysis and Additional Data Confirming the Common Founder Mutations.” Annals of Hematology 97 (6): 1061–69. doi:10.1007/s00277-018-3264-2.