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Feichtinger RG, Preisel M, Brugger K, Wortmann SB, Mayr JA. 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. Genes. 2023; 14(6):1217. https://doi.org/10.3390/genes14061217

Feichtinger, René G., Martin Preisel, Karin Brugger, Saskia B. Wortmann, and Johannes A. Mayr. 2023. "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" Genes 14, no. 6: 1217. https://doi.org/10.3390/genes14061217

Feichtinger, R. G., Preisel, M., Brugger, K., Wortmann, S. B., & Mayr, J. A. (2023). 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. Genes, 14(6), 1217. https://doi.org/10.3390/genes14061217