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Figure 1 | Molecular Autism

Figure 1

From: Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci

Figure 1

A deletion of approximately 70 kb encompassing two exons (3,4) from the NRXN1 gene (alpha-1-isoform). Previously reported NRXN1 CNV events in ASD cases are shown mapped below [3840, 4249]. A subset of NRXN1 structural variants reported in individuals with mild to severe intellectual disability is also depicted [49]. Solid lines indicate deletions (majority) and dashed lines indicate duplication events.

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