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- W4245087365 abstract "The discovery of the highly recurrent, gain-of-function MYD88L265P mutation, harbored by more than 90% of patients with Waldenstrom macroglobulinemia (WM), was critical in deepening our understanding of the disease biology" @default.
- W4245087365 created "2022-05-12" @default.
- W4245087365 date "2021-02-25" @default.
- W4245087365 modified "2023-09-27" @default.
- W4245087365 title "Frontline Treatment of Symptomatic MYD88L265P-Mutant Waldenstrom Macroglobulinemia" @default.
- W4245087365 doi "https://doi.org/10.1200/adn.21.200486" @default.
- W4245087365 hasPublicationYear "2021" @default.
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