Park, S.; So, M.-K.; Cho, M.-S.; Kim, D.-Y.; Huh, J.
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 2021, 11, 1644.
https://doi.org/10.3390/diagnostics11091644
AMA Style
Park S, So M-K, Cho M-S, Kim D-Y, Huh J.
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. 2021; 11(9):1644.
https://doi.org/10.3390/diagnostics11091644
Chicago/Turabian Style
Park, Sholhui, Min-Kyung So, Min-Sun Cho, Dae-Young Kim, and Jungwon Huh.
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 11, no. 9: 1644.
https://doi.org/10.3390/diagnostics11091644
APA Style
Park, S., So, M.-K., Cho, M.-S., Kim, D.-Y., & 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, 11(9), 1644.
https://doi.org/10.3390/diagnostics11091644