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• W2056777053 abstract "The V617F mutation, which causes the substitution of phenylalanine for valine at position 617 of the Janus kinase (JAK) 2 gene (JAK2), is often present in patients with polycythemia vera, essential thrombocythemia, and idiopathic myelofibrosis. However, the molecular basis of these myeloproliferative disorders in patients without the V617F mutation is unclear." @default.
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• W2056777053 date "2007-02-01" @default.
• W2056777053 modified "2023-10-17" @default.
• W2056777053 title "<i>JAK2</i>Exon 12 Mutations in Polycythemia Vera and Idiopathic Erythrocytosis" @default.
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• W2056777053 doi "https://doi.org/10.1056/nejmoa065202" @default.
• W2056777053 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/2873834" @default.
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