Mutation analysis of the NRXN1 gene in autism spectrum disorders
The aim of this study was to identify the sequence mutations in the Neurexin 1 (NRXN1) gene that has been considered as one of the strong candidate genes.A total of 30 children and adolescents great neck chisels (aged 3-18) with non syndromic autism were enrolled this study.Sequencing of the coding exons and the exon-intron boundaries of the NRXN1