Coexistence of Primary Myelofibrosis and Paroxysmal Nocturnal Hemoglobinuria Clone with JAK2 V617F, U2AF1 and SETBP1 Mutations: A Case Report and Brief Review of Literature.
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| Title: | Coexistence of Primary Myelofibrosis and Paroxysmal Nocturnal Hemoglobinuria Clone with JAK2 V617F, U2AF1 and SETBP1 Mutations: A Case Report and Brief Review of Literature. |
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| Authors: | Park, Sholhui1 (AUTHOR) solheepark@ewha.ac.kr, So, Min-Kyung1 (AUTHOR) mkso79@gmail.com, Cho, Min-Sun2 (AUTHOR) mcho1124@ewha.ac.kr, Kim, Dae-Young3 (AUTHOR) rubatokim@gmail.com, Huh, Jungwon1 (AUTHOR) JungWonH@ewha.ac.kr |
| Source: | Diagnostics (2075-4418). Sep2021, Vol. 11 Issue 9, p1644. 1p. |
| Database: | Academic Search Ultimate |
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| ISSN: | 20754418 |
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| DOI: | 10.3390/diagnostics11091644 |
