APA (7th ed.) Citation

JR, L., K, G., KL, H., HO, H., H, S., J, H., . . . S, S. (2016). Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. Neurology, 86(23), 2171. https://doi.org/10.1212/WNL.0000000000002740

Chicago Style (17th ed.) Citation

JR, Lemke, et al. "Delineating the GRIN1 Phenotypic Spectrum: A Distinct Genetic NMDA Receptor Encephalopathy." Neurology 86, no. 23 (2016): 2171. https://doi.org/10.1212/WNL.0000000000002740.

MLA (9th ed.) Citation

JR, Lemke, et al. "Delineating the GRIN1 Phenotypic Spectrum: A Distinct Genetic NMDA Receptor Encephalopathy." Neurology, vol. 86, no. 23, 2016, p. 2171, https://doi.org/10.1212/WNL.0000000000002740.