APA (7th ed.) Citation

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

Chicago Style (17th ed.) Citation

Feichtinger, René G., Martin Preisel, Karin Brugger, Saskia B. Wortmann, and Johannes A. Mayr. "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 (2023): 1217. https://doi.org/10.3390/genes14061217.

MLA (9th ed.) Citation

Feichtinger, René G., et al. "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, vol. 14, no. 6, 2023, p. 1217, https://doi.org/10.3390/genes14061217.