Autoimmune lymphoproliferative syndrome caused by a homozygous FasL mutation that disrupts FasL assembly

J Allergy Clin Immunol. 2016 Jan;137(1):324-327.e2. doi: 10.1016/j.jaci.2015.08.025. Epub 2015 Oct 10.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autoimmune Lymphoproliferative Syndrome / genetics*
  • CHO Cells
  • Cricetulus
  • Fas Ligand Protein / genetics*
  • Fas Ligand Protein / metabolism
  • Female
  • Homozygote
  • Humans
  • Infant
  • Leukocytes, Mononuclear / metabolism
  • Male
  • Mutation

Substances

  • FASLG protein, human
  • Fas Ligand Protein