De novo autosomal dominant mutation in SYNGAP1

Autism Res. 2011 Apr;4(2):155-6. doi: 10.1002/aur.198.
No abstract available

Publication types

  • Review

MeSH terms

  • Autistic Disorder / genetics*
  • Female
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Male
  • ras GTPase-Activating Proteins / genetics*

Substances

  • SYNGAP1 protein, human
  • ras GTPase-Activating Proteins