APA (7th ed.) Citation

RG, F., M, P., K, B., SB, W., & JA, M. (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), . https://doi.org/10.3390/genes14061217

Chicago Style (17th ed.) Citation

RG, Feichtinger, Preisel M, Brugger K, Wortmann SB, and 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 14, no. 6 (2023). https://doi.org/10.3390/genes14061217.

MLA (9th ed.) Citation

RG, Feichtinger, 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, https://doi.org/10.3390/genes14061217.