APA (7th ed.) Citation

Zdziarska, J., Wypasek, E., Iwaniec, T., Vilar, R., Neerman‐Arbez, M., & Undas, A. (2021). Afibrinogenemia caused by a novel homozygous missense mutation, FGB p.Cys241Tyr, in a male patient with recurrent intracranial bleeding: Case report and review of literature. Haemophilia, 27(1), 26. https://doi.org/10.1111/hae.14211

Chicago Style (17th ed.) Citation

Zdziarska, Joanna, Ewa Wypasek, Teresa Iwaniec, Rui Vilar, Marguerite Neerman‐Arbez, and Anetta Undas. "Afibrinogenemia Caused by a Novel Homozygous Missense Mutation, FGB P.Cys241Tyr, in a Male Patient with Recurrent Intracranial Bleeding: Case Report and Review of Literature." Haemophilia 27, no. 1 (2021): 26. https://doi.org/10.1111/hae.14211.

MLA (9th ed.) Citation

Zdziarska, Joanna, et al. "Afibrinogenemia Caused by a Novel Homozygous Missense Mutation, FGB P.Cys241Tyr, in a Male Patient with Recurrent Intracranial Bleeding: Case Report and Review of Literature." Haemophilia, vol. 27, no. 1, 2021, p. 26, https://doi.org/10.1111/hae.14211.