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14. The genomic landscape of Waldenstrom macroglobulinemia is characterized by highly recurring MYD88 and WHIM-like CXCR4 mutations, and small somatic deletions associated with B-cell lymphomagenesis. Hunter ZR; Xu L; Yang G; Zhou Y; Liu X; Cao Y; Manning RJ; Tripsas C; Patterson CJ; Sheehy P; Treon SP Blood; 2014 Mar; 123(11):1637-46. PubMed ID: 24366360 [TBL] [Abstract][Full Text] [Related]
15. [Gene mutations connected to Waldenstöm macroglobulinemia]. Kutálková K; Sedlaříková L; Adam Z; Ševčíková S Vnitr Lek; 2016 Jan; 62(1):40-3. PubMed ID: 26967235 [TBL] [Abstract][Full Text] [Related]
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17. Characteristics of Waldenström Macroglobulinemia in Korean Patients According to Mutational Status of MYD88 and CXCR4: Analysis Using Ultra-Deep Sequencing. Shin DW; Kim SM; Kim JA; Park HS; Hwang SM; Im K; Kim S; Kim J; Kwon S; Yoon SS; Lee DS Clin Lymphoma Myeloma Leuk; 2019 Aug; 19(8):e496-e505. PubMed ID: 31221512 [TBL] [Abstract][Full Text] [Related]
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19. Somatic mutations in MYD88 and CXCR4 are determinants of clinical presentation and overall survival in Waldenstrom macroglobulinemia. Treon SP; Cao Y; Xu L; Yang G; Liu X; Hunter ZR Blood; 2014 May; 123(18):2791-6. PubMed ID: 24553177 [TBL] [Abstract][Full Text] [Related]