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    • Home
    • Diagnostics
      • Polycythemia Vera
      • Essential Thrombocythemia
      • Primary Myelofibrosis
      • Congenital Erythrocytosis
      • Hereditary Thrombocytosis
    • Molecular analyses
      • JAK2V617F
      • JAK2 Exon 12 mutations
      • Mpl/TPO_Receptor
      • Calreticulin (CALR)
      • Other genes mutated in MPN
      • EPO-Receptor
      • Oxygen sensing pathway genes
      • THPO
    • Events
    • Useful links
    • Members
    • Registration
    • INTRANET

      Mpl/TPO_Receptor

      • Home
      • Mpl/TPO_Receptor

      Mpl/TPO_Receptor

      MPL encodes for the receptor for thrombopoietin. It has been found mutated in hereditary as well as acquired thrombocytosis. The mutations occur mainly in exon 10 of MPL, affecting S505 or W515.

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      Organization committee:

      Danijela Leković, Andrija Bogdanović, Nataša Debeljak and Vladan Čokić
      Medical faculty, University of Belgrade
      Institute for medical research, University of Belgrade
      Belgrade, Serbia

      Former EU-sponsored COST Action BM0902 (2009-2013), a network of experts … “

      by MPN&MPNr-EuroNet.

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