Lethal digenic mutations in the K + channels Kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay.

MLA

Hasan, Sonia, et al. “Lethal Digenic Mutations in the K + Channels Kir4.1 (KCNJ10) and SLACK (KCNT1) Associated with Severe-Disabling Seizures and Neurodevelopmental Delay.” Journal of Neurophysiology, vol. 118, no. 4, Oct. 2017, pp. 2402–11. EBSCOhost, https://doi.org/10.1152/jn.00284.2017.

APA

Hasan, S., Balobaid, A., Grottesi, A., Dabbagh, O., Cenciarini, M., Rawashdeh, R., Al-Sagheir, A., Bove, C., Macchioni, L., Pessia, M., Al-Owain, M., & D, A. M. C. (2017). Lethal digenic mutations in the K + channels Kir4.1 (KCNJ10) and SLACK (KCNT1) associated with severe-disabling seizures and neurodevelopmental delay. Journal of Neurophysiology, 118(4), 2402–2411. https://doi.org/10.1152/jn.00284.2017

Chicago

Hasan, Sonia, Ameera Balobaid, Alessandro Grottesi, Omar Dabbagh, Marta Cenciarini, Rifaat Rawashdeh, Afaf Al-Sagheir, et al. 2017. “Lethal Digenic Mutations in the K + Channels Kir4.1 (KCNJ10) and SLACK (KCNT1) Associated with Severe-Disabling Seizures and Neurodevelopmental Delay.” Journal of Neurophysiology 118 (4): 2402–11. doi:10.1152/jn.00284.2017.