Platelet functional abnormalities and clinical presentation in pediatric patients with germline RUNX1, ANKRD26, and ETV6 mutations

Haematologica. 2022 Oct 1;107(10):2511-2516. doi: 10.3324/haematol.2022.281340.
No abstract available

MeSH terms

  • Blood Platelet Disorders* / diagnosis
  • Blood Platelet Disorders* / genetics
  • Child
  • Core Binding Factor Alpha 2 Subunit* / genetics
  • Germ Cells
  • Humans
  • Intercellular Signaling Peptides and Proteins / genetics
  • Mutation
  • Oncogene Proteins, Fusion / genetics

Substances

  • ANKRD26 protein, human
  • Core Binding Factor Alpha 2 Subunit
  • Intercellular Signaling Peptides and Proteins
  • Oncogene Proteins, Fusion
  • RUNX1 protein, human

Grants and funding

Funding: This work was supported by a grant from the Charitable Foundation “Science for Children” in the Russian Federation.