ASXL1 mutated chronic myelomonocytic leukemia in a patient with familial thrombocytopenia secondary to germline mutation in ANKRD26

Παρόμοια τεκμήρια

• Prognostic interaction between ASXL1 and TET2 mutations in chronic myelomonocytic leukemia
  ανά: Patnaik, M M, κ.ά.
  Έκδοση: (2016)
• EZH2 mutations in chronic myelomonocytic leukemia cluster with ASXL1 mutations and their co-occurrence is prognostically detrimental
  ανά: Patnaik, Mrinal M., κ.ά.
  Έκδοση: (2018)
• Inherited Thrombocytopenia Caused by Germline ANKRD26 Mutation Should Be Considered in Young Patients With Suspected Myelodysplastic Syndrome
  ανά: Kewan, Tariq, κ.ά.
  Έκδοση: (2020)
• Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation
  ανά: Bluteau, Dominique, κ.ά.
  Έκδοση: (2014)
• A new family with a germline ANKRD26 mutation and predisposition to myeloid malignancies
  ανά: Marquez, Rafael, κ.ά.
  Έκδοση: (2014)