MECP2 mutation in a boy with language disorder and schizophrenia

Am J Psychiatry. 2002 Jan;159(1):148-9. doi: 10.1176/appi.ajp.159.1.148-a.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Alanine / genetics
  • Amino Acid Substitution / genetics
  • Child
  • Chromosomal Proteins, Non-Histone*
  • DNA-Binding Proteins / genetics*
  • Follow-Up Studies
  • Humans
  • Language Development Disorders / diagnosis
  • Language Development Disorders / genetics*
  • Language Development Disorders / psychology
  • Male
  • Methyl-CpG-Binding Protein 2
  • Mutation, Missense / genetics*
  • Repressor Proteins*
  • Schizophrenia, Childhood / diagnosis
  • Schizophrenia, Childhood / genetics*
  • Valine / genetics

Substances

  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • MECP2 protein, human
  • Methyl-CpG-Binding Protein 2
  • Repressor Proteins
  • Valine
  • Alanine