APA (7th ed.) Citation

L, A., W, S., SV, T., RH, C., SJ, N., K, G., . . . DK, P. (2018). Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses. Journal of medical genetics, 55(9), 607. https://doi.org/10.1136/jmedgenet-2018-105319

Chicago Style (17th ed.) Citation

L, Addis, et al. "Identification of New Risk Factors for Rolandic Epilepsy: CNV at Xp22.31 and Alterations at Cholinergic Synapses." Journal of Medical Genetics 55, no. 9 (2018): 607. https://doi.org/10.1136/jmedgenet-2018-105319.

MLA (9th ed.) Citation

L, Addis, et al. "Identification of New Risk Factors for Rolandic Epilepsy: CNV at Xp22.31 and Alterations at Cholinergic Synapses." Journal of Medical Genetics, vol. 55, no. 9, 2018, p. 607, https://doi.org/10.1136/jmedgenet-2018-105319.