A case of recurrent encephalopathy with SCN2A missense mutation.

MLA

Fukasawa, Tatsuya, et al. “A Case of Recurrent Encephalopathy with SCN2A Missense Mutation.” Brain & Development, vol. 37, no. 6, June 2015, pp. 631–34. EBSCOhost, https://doi.org/10.1016/j.braindev.2014.10.001.

APA

Fukasawa, T., Kubota, T., Negoro, T., Saitoh, M., Mizuguchi, M., Ihara, Y., Ishii, A., & Hirose, S. (2015). A case of recurrent encephalopathy with SCN2A missense mutation. Brain & Development, 37(6), 631–634. https://doi.org/10.1016/j.braindev.2014.10.001

Chicago

Fukasawa, Tatsuya, Tetsuo Kubota, Tamiko Negoro, Makiko Saitoh, Masashi Mizuguchi, Yukiko Ihara, Atsushi Ishii, and Shinichi Hirose. 2015. “A Case of Recurrent Encephalopathy with SCN2A Missense Mutation.” Brain & Development 37 (6): 631–34. doi:10.1016/j.braindev.2014.10.001.