APA (7th ed.) Citation

MV, C., MA, H., S, S., M, C., HE, A., ML, E., . . . TD, W. (2021). Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function. Haematologica, 106(5), 1423. https://doi.org/10.3324/haematol.2019.235895

Chicago Style (17th ed.) Citation

MV, Chan, et al. "Identification of a Homozygous Recessive Variant in PTGS1 Resulting in a Congenital Aspirin-like Defect in Platelet Function." Haematologica 106, no. 5 (2021): 1423. https://doi.org/10.3324/haematol.2019.235895.

MLA (9th ed.) Citation

MV, Chan, et al. "Identification of a Homozygous Recessive Variant in PTGS1 Resulting in a Congenital Aspirin-like Defect in Platelet Function." Haematologica, vol. 106, no. 5, 2021, p. 1423, https://doi.org/10.3324/haematol.2019.235895.