Cite
Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes.
MLA
Scala, Marcello, et al. “Variant-Specific Changes in RAC3 Function Disrupt Corticogenesis in Neurodevelopmental Phenotypes.” Brain : A Journal of Neurology, vol. 145, no. 9, Sept. 2022, pp. 3308–27. EBSCOhost, https://doi.org/10.1093/brain/awac106.
APA
Scala, M., Nishikawa, M., Ito, H., Tabata, H., Khan, T., Accogli, A., Davids, L., Ruiz, A., Chiurazzi, P., Cericola, G., Schulte, B., Monaghan, K. G., Begtrup, A., Torella, A., Pinelli, M., Denommé-Pichon, A. S., Vitobello, A., Racine, C., Mancardi, M. M., … Nagata, K. I. (2022). Variant-specific changes in RAC3 function disrupt corticogenesis in neurodevelopmental phenotypes. Brain : A Journal of Neurology, 145(9), 3308–3327. https://doi.org/10.1093/brain/awac106
Chicago
Scala, Marcello, Masashi Nishikawa, Hidenori Ito, Hidenori Tabata, Tayyaba Khan, Andrea Accogli, Laura Davids, et al. 2022. “Variant-Specific Changes in RAC3 Function Disrupt Corticogenesis in Neurodevelopmental Phenotypes.” Brain : A Journal of Neurology 145 (9): 3308–27. doi:10.1093/brain/awac106.