First characterization of platelet secretion defect in patients with familial hemophagocytic lymphohistiocytosis type 3 (FHL-3)

Blood. 2015 Jan 8;125(2):412-4. doi: 10.1182/blood-2014-07-587568.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Blood Platelets / metabolism
  • Blood Platelets / pathology*
  • Flow Cytometry
  • Humans
  • Infant
  • Lymphohistiocytosis, Hemophagocytic / genetics
  • Lymphohistiocytosis, Hemophagocytic / metabolism
  • Lymphohistiocytosis, Hemophagocytic / pathology*
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism
  • Mutation

Substances

  • Membrane Proteins
  • UNC13D protein, human

Supplementary concepts

  • Hemophagocytic lymphohistiocytosis, familial, 3