Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome

Am J Hum Genet. 2008 Jun;82(6):1385. doi: 10.1016/j.ajhg.2008.04.021.
No abstract available

Publication types

  • Case Reports
  • Comment

MeSH terms

  • Autistic Disorder / genetics
  • Cell Adhesion Molecules, Neuronal / genetics*
  • Child
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 3 / genetics*
  • Contactins
  • Developmental Disabilities / genetics*
  • Humans
  • Male
  • Syndrome
  • Translocation, Genetic

Substances

  • CNTN4 protein, human
  • Cell Adhesion Molecules, Neuronal
  • Contactins