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<i>NLGN3</i> autism variants have distinct functional impact on synapses and sleep behavior in <i>Drosophila</i>
Neuroligin-3 (NLGN3) was first identified as a X-linked risk gene associated with autism spectrum disorder (ASD). Most reported variants are identified in males who inherited their variants from an unaffected mother, but de novo variants have also been identified in both affected heterozygous femal
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