Association of INPP1, PIK3CG, and TSC2 gene variants with autistic disorder: implications for phosphatidylinositol signalling in autism

J Med Genet. 2003 Nov;40(11):e119. doi: 10.1136/jmg.40.11.e119.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autistic Disorder / genetics*
  • Child
  • Class Ib Phosphatidylinositol 3-Kinase
  • Female
  • Genetic Variation / genetics*
  • Haplotypes / genetics
  • Humans
  • Isoenzymes / genetics
  • Isoenzymes / physiology*
  • Linkage Disequilibrium / genetics
  • Male
  • Mathematical Computing
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphatidylinositol 3-Kinases / physiology*
  • Phosphatidylinositols / genetics
  • Phosphatidylinositols / physiology*
  • Phosphoric Monoester Hydrolases / genetics
  • Phosphoric Monoester Hydrolases / physiology*
  • Polymorphism, Single Nucleotide / genetics
  • Repressor Proteins / genetics
  • Repressor Proteins / physiology*
  • Signal Transduction / genetics*
  • Tuberous Sclerosis Complex 2 Protein
  • Tumor Suppressor Proteins

Substances

  • Isoenzymes
  • Phosphatidylinositols
  • Repressor Proteins
  • TSC2 protein, human
  • Tuberous Sclerosis Complex 2 Protein
  • Tumor Suppressor Proteins
  • Phosphatidylinositol 3-Kinases
  • Class Ib Phosphatidylinositol 3-Kinase
  • PIK3CG protein, human
  • Phosphoric Monoester Hydrolases
  • inositol-1,4-bisphosphate 1-phosphatase

Associated data

  • OMIM/209850