Kahle, K. T., Merner, N. D., Friedel, P., Silayeva, L., Liang, B., Khanna, A., . . . Rouleau, G. A. (2014). Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy. EMBO reports, 15(7), 766-774. https://doi.org/10.15252/embr.201438840
Chicago Style (17th ed.) CitationKahle, Kristopher T., et al. "Genetically Encoded Impairment of Neuronal KCC2 Cotransporter Function in Human Idiopathic Generalized Epilepsy." EMBO Reports 15, no. 7 (2014): 766-774. https://doi.org/10.15252/embr.201438840.
MLA (9th ed.) CitationKahle, Kristopher T., et al. "Genetically Encoded Impairment of Neuronal KCC2 Cotransporter Function in Human Idiopathic Generalized Epilepsy." EMBO Reports, vol. 15, no. 7, 2014, pp. 766-774, https://doi.org/10.15252/embr.201438840.