No association between the XPD Lys751Gln (rs13181) polymorphism and disease phenotype or leukemic transformation in primary myelofibrosis

Ítems similars

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  per: SAMSON, MANI, et al.
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• JAK2 V617F Genotype Is a Strong Determinant of Blast Transformation in Primary Myelofibrosis
  per: Barosi, Giovanni, et al.
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• Evidence that Prefibrotic Myelofibrosis Is Aligned along a Clinical and Biological Continuum Featuring Primary Myelofibrosis
  per: Barosi, Giovanni, et al.
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• Associations Between XPD Lys751Gln Polymorphism and Leukemia: A Meta-Analysis
  per: Wen, Min, et al.
  Publicat: (2018)
• Constitutive STAT5 phosphorylation in CD34(+) cells of patients with primary myelofibrosis: Correlation with driver mutation status and disease severity
  per: Abbà, Carlotta, et al.
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