Case Report—An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions. - Feichtinger, René G.; Preisel, Martin; Brugger, Karin; Wortmann, Saskia B.; Mayr, Johannes A. (Genes, 2023)