TWO SITTINGS OF AUTOLOGOUS BONE MARROW STEM CELLS WITHIN TWO YEARS IN A CASE OF ISCHEMIC CARDIOMYOPATHY





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 ls32a804nmnxgo 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

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