Cite
A de novo p.Arg756Cys mutation in ATP1A3 causes a distinct phenotype with prolonged weakness and encephalopathy triggered by fever.
MLA
Nakamura, Yuji, et al. “A de Novo p.Arg756Cys Mutation in ATP1A3 Causes a Distinct Phenotype with Prolonged Weakness and Encephalopathy Triggered by Fever.” Brain & Development, vol. 40, no. 3, Mar. 2018, pp. 222–25. EBSCOhost, https://doi.org/10.1016/j.braindev.2017.09.010.
APA
Nakamura, Y., Hattori, A., Nakashima, M., Ieda, D., Hori, I., Negishi, Y., Ando, N., Matsumoto, N., & Saitoh, S. (2018). A de novo p.Arg756Cys mutation in ATP1A3 causes a distinct phenotype with prolonged weakness and encephalopathy triggered by fever. Brain & Development, 40(3), 222–225. https://doi.org/10.1016/j.braindev.2017.09.010
Chicago
Nakamura, Yuji, Ayako Hattori, Mitsuko Nakashima, Daisuke Ieda, Ikumi Hori, Yutaka Negishi, Naoki Ando, Naomichi Matsumoto, and Shinji Saitoh. 2018. “A de Novo p.Arg756Cys Mutation in ATP1A3 Causes a Distinct Phenotype with Prolonged Weakness and Encephalopathy Triggered by Fever.” Brain & Development 40 (3): 222–25. doi:10.1016/j.braindev.2017.09.010.