APA (7th ed.) Citation

Chan, M. V., Hayman, M. A., Sivapalaratnam, S., Crescente, M., Allan, H. E., Edin, M. L., . . . Warner, T. D. (2021). Identification of a homozygous recessive variant in PTGS1 resulting in a congenital aspirin-like defect in platelet function. Haematologica (Roma), 106(5), 1423-1432. https://doi.org/10.3324/haematol.2019.235895

Chicago Style (17th ed.) Citation

Chan, Melissa V., et al. "Identification of a Homozygous Recessive Variant in PTGS1 Resulting in a Congenital Aspirin-like Defect in Platelet Function." Haematologica (Roma) 106, no. 5 (2021): 1423-1432. https://doi.org/10.3324/haematol.2019.235895.

MLA (9th ed.) Citation

Chan, Melissa V., et al. "Identification of a Homozygous Recessive Variant in PTGS1 Resulting in a Congenital Aspirin-like Defect in Platelet Function." Haematologica (Roma), vol. 106, no. 5, 2021, pp. 1423-1432, https://doi.org/10.3324/haematol.2019.235895.