CCDC22: a novel candidate gene for syndromic X-linked intellectual disability

Mol Psychiatry. 2012 Jan;17(1):4-7. doi: 10.1038/mp.2011.95. Epub 2011 Aug 9.
No abstract available

Publication types

  • Letter

MeSH terms

  • Carrier Proteins / metabolism
  • Case-Control Studies
  • Chromosomes, Human, X*
  • Cohort Studies
  • DNA-Binding Proteins
  • Genetic Diseases, X-Linked*
  • Genetic Predisposition to Disease / genetics*
  • Genome-Wide Association Study
  • Humans
  • Intellectual Disability / genetics*
  • Male
  • Mutation / genetics*
  • Nuclear Proteins / metabolism
  • Phenotype
  • Proteins / genetics*
  • RNA, Messenger / metabolism

Substances

  • CCDC22 protein, human
  • Carrier Proteins
  • DNA-Binding Proteins
  • Nuclear Proteins
  • PQBP1 protein, human
  • Proteins
  • RNA, Messenger