Novel PIK3CD mutations affecting N-terminal residues of p110δ cause activated PI3Kδ syndrome (APDS) in humans

J Allergy Clin Immunol. 2017 Oct;140(4):1152-1156.e10. doi: 10.1016/j.jaci.2017.03.026. Epub 2017 Apr 13.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Class I Phosphatidylinositol 3-Kinases / genetics*
  • Female
  • Humans
  • Immunologic Deficiency Syndromes / genetics*
  • Male
  • Mutation

Substances

  • Class I Phosphatidylinositol 3-Kinases
  • PIK3CD protein, human