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Article

Mutation analysis of the NRXN1 gene in autism spectrum disorders

1 Dec 2016

Abstract excerpt

Abstract 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 (aged 3-18) with non syndromic autism were enrolled this study. Sequencing of the coding exons and the exon-intron boundaries of the NRXN1 gene was performed. Two known mutations were described in two different...

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PMID: 28289584
DOI: 10.1515/bjmg-2016-0031

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