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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.
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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  Data: 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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PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=152688133
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        Value: 10.3390/diagnostics11091644
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        Text: English
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      – TitleFull: 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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            NameFull: Park, Sholhui
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            NameFull: So, Min-Kyung
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            NameFull: Cho, Min-Sun
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            NameFull: Kim, Dae-Young
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            NameFull: Huh, Jungwon
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            – D: 01
              M: 09
              Text: Sep2021
              Type: published
              Y: 2021
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              Value: 11
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              Value: 9
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