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- W1977522017 abstract "In this issue of Blood, Lambert and colleagues propose a new disease paradigm for one of the CMPNs, ET. They show that in ET, the JAK2 V617F mutation occurs as multiple independent events.1 Using a common single nucleotide polymorphism located in the JAK2 gene, they demonstrate that the mutation commonly occurs on both alleles in ET. The authors argue that, because of these new findings, the presence of the JAK2 V617F in ET should not be equated with malignant disease." @default.
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- W1977522017 date "2009-10-01" @default.
- W1977522017 modified "2023-10-01" @default.
- W1977522017 title "Same mutation, different allele" @default.
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- W1977522017 doi "https://doi.org/10.1182/blood-2009-07-229906" @default.
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