Evidence of neurocognitive and resting state functional connectivity differences in carriers of NRXN1 deletions
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Background: NRXN1 deletion (NRXN1 del) is a rare copy number variant associated with several neurodevelopmental, neuropsychiatric, and cognitive outcomes. The NRXN1 gene encodes for a pre-synaptic cell adhesion molecule that is i... ...
