APA (7th ed.) Citation

Y, Y., J, J., YN, L., Y, L., H, C., E, N., . . . M, C. (2017). GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy. Annals of neurology, 82(3), 466. https://doi.org/10.1002/ana.25032

Chicago Style (17th ed.) Citation

Y, Yoo, et al. "GABBR2 Mutations Determine Phenotype in Rett Syndrome and Epileptic Encephalopathy." Annals of Neurology 82, no. 3 (2017): 466. https://doi.org/10.1002/ana.25032.

MLA (9th ed.) Citation

Y, Yoo, et al. "GABBR2 Mutations Determine Phenotype in Rett Syndrome and Epileptic Encephalopathy." Annals of Neurology, vol. 82, no. 3, 2017, p. 466, https://doi.org/10.1002/ana.25032.