Coexistence of Primary Myelofibrosis and Paroxysmal Nocturnal Hemoglobinuria Clone with JAK2 V617F, U2AF1 and SETBP1 Mutations: A Case Report and Brief Review of Literature. - Park, Sholhui; So, Min-Kyung; Cho, Min-Sun; Kim, Dae-Young; Huh, Jungwon (Diagnostics (2075-4418), 2021)