APA (7th ed.) Citation

Park, S., So, M., Cho, M., Kim, D., & Huh, J. (2021). Coexistence of Primary Myelofibrosis and Paroxysmal Nocturnal Hemoglobinuria Clone with JAK2 V617F, U2AF1 and SETBP1 Mutations: A Case Report and Brief Review of Literature. Diagnostics (2075-4418), 11(9), 1644. https://doi.org/10.3390/diagnostics11091644

Chicago Style (17th ed.) Citation

Park, Sholhui, Min-Kyung So, Min-Sun Cho, Dae-Young Kim, and Jungwon Huh. "Coexistence of Primary Myelofibrosis and Paroxysmal Nocturnal Hemoglobinuria Clone with JAK2 V617F, U2AF1 and SETBP1 Mutations: A Case Report and Brief Review of Literature." Diagnostics (2075-4418) 11, no. 9 (2021): 1644. https://doi.org/10.3390/diagnostics11091644.

MLA (9th ed.) Citation

Park, Sholhui, et al. "Coexistence of Primary Myelofibrosis and Paroxysmal Nocturnal Hemoglobinuria Clone with JAK2 V617F, U2AF1 and SETBP1 Mutations: A Case Report and Brief Review of Literature." Diagnostics (2075-4418), vol. 11, no. 9, 2021, p. 1644, https://doi.org/10.3390/diagnostics11091644.