Cite
GRIN1 variants associated with neurodevelopmental disorders reveal channel gating pathomechanisms.
MLA
Ragnarsson, Lotten, et al. “GRIN1 Variants Associated with Neurodevelopmental Disorders Reveal Channel Gating Pathomechanisms.” Epilepsia (Series 4), vol. 64, no. 12, Dec. 2023, pp. 3377–88. EBSCOhost, https://doi.org/10.1111/epi.17776.
APA
Ragnarsson, L., Zhang, Z., Das, S. S., Tran, P., Andersson, Å., des Portes, V., Desmettre, A. C., Remerand, G., Labalme, A., Chatron, N., Sanlaville, D., Lesca, G., Anggono, V., Vetter, I., & Keramidas, A. (2023). GRIN1 variants associated with neurodevelopmental disorders reveal channel gating pathomechanisms. Epilepsia (Series 4), 64(12), 3377–3388. https://doi.org/10.1111/epi.17776
Chicago
Ragnarsson, Lotten, Zihan Zhang, Sooraj S. Das, Poanna Tran, Åsa Andersson, Vincent des Portes, Altuzarra, Cecilia Desmettre, et al. 2023. “GRIN1 Variants Associated with Neurodevelopmental Disorders Reveal Channel Gating Pathomechanisms.” Epilepsia (Series 4) 64 (12): 3377–88. doi:10.1111/epi.17776.