No association of polymorphisms in the CDK5, NDEL1, and LIS1 with autism in Chinese Han population

Psychiatry Res. 2011 Dec 30;190(2-3):369-71. doi: 10.1016/j.psychres.2011.08.004. Epub 2011 Sep 3.

Abstract

Autism is a pervasive neurodevelopmental disorder. CDK5 (cyclin-dependent kinase 5) and its interacting molecules are involved in neurodevelopment. We performed a family-based association analysis between CDK5, NDEL1, and LIS1 polymorphisms and autism in a Chinese Han population. Our study did not detect a significant association. It indicated that common genetic variations in these genes might not play a role in the genetic predisposition to autism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / genetics*
  • Adolescent
  • Asian People / ethnology
  • Asian People / genetics
  • Autistic Disorder / genetics*
  • Carrier Proteins / genetics*
  • Child
  • Child, Preschool
  • China / epidemiology
  • China / ethnology
  • Cyclin-Dependent Kinase 5 / genetics*
  • Family Health
  • Female
  • Genetic Association Studies
  • Genotype
  • Humans
  • Male
  • Microtubule-Associated Proteins / genetics*
  • Polymorphism, Genetic / genetics*

Substances

  • Carrier Proteins
  • Microtubule-Associated Proteins
  • NDEL1 protein, human
  • Cyclin-Dependent Kinase 5
  • CDK5 protein, human
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase
  • PAFAH1B1 protein, human