Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX)

J Med Genet. 2001 Dec;38(12):874-6. doi: 10.1136/jmg.38.12.874.
No abstract available

Publication types

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

MeSH terms

  • Asian People / genetics
  • Base Sequence
  • Child
  • Child, Preschool
  • DNA Mutational Analysis
  • DNA-Binding Proteins / genetics*
  • Diabetes Mellitus, Type 1 / genetics*
  • Female
  • Forkhead Transcription Factors
  • Genetic Linkage / genetics
  • Humans
  • Infant
  • Infant, Newborn
  • Infant, Newborn, Diseases / genetics*
  • Japan
  • Kidney Diseases / genetics*
  • Male
  • Mutation / genetics*
  • Polyendocrinopathies, Autoimmune / genetics*
  • Syndrome
  • Thyroiditis, Autoimmune / genetics*
  • X Chromosome / genetics

Substances

  • DNA-Binding Proteins
  • FOXP3 protein, human
  • Forkhead Transcription Factors