A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders

Mol Psychiatry. 2011 Mar;16(3):238-9. doi: 10.1038/mp.2010.59. Epub 2010 May 18.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child
  • Child Development Disorders, Pervasive / complications
  • Child Development Disorders, Pervasive / genetics*
  • Frameshift Mutation / genetics*
  • Humans
  • Male
  • RNA-Binding Proteins / genetics*
  • Schizophrenia, Childhood / complications
  • Schizophrenia, Childhood / genetics*
  • Young Adult

Substances

  • RNA-Binding Proteins
  • UPF3B protein, human