A Novel Missense Mutation Affecting the N-terminal Domain of SAP Protein in X-linked Lymphoproliferative Disease

J Pediatr Hematol Oncol. 2019 Nov;41(8):e550-e551. doi: 10.1097/MPH.0000000000001585.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Child
  • Humans
  • Lymphoproliferative Disorders / genetics*
  • Male
  • Mutation, Missense*
  • Protein Domains
  • Signaling Lymphocytic Activation Molecule Associated Protein / genetics*

Substances

  • SH2D1A protein, human
  • Signaling Lymphocytic Activation Molecule Associated Protein