APA

Kanemasa H., Fukai R., Sakai Y., Torio M., Miyake N., Lee S., Ono H., Akamine S., Nishiyama K., Sanefuji M., Ishizaki Y., Torisu H., Saitsu H., Matsumoto N. & Hara T. (20161230). De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis. : BMC neurology.

Chicago

Kanemasa Hikaru, Fukai Ryoko, Sakai Yasunari, Torio Michiko, Miyake Noriko, Lee Sooyoung, Ono Hiroaki, Akamine Satoshi, Nishiyama Kei, Sanefuji Masafumi, Ishizaki Yoshito, Torisu Hiroyuki, Saitsu Hirotomo, Matsumoto Naomichi and Hara Toshiro. 20161230. De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis. : BMC neurology.

Harvard

Kanemasa H., Fukai R., Sakai Y., Torio M., Miyake N., Lee S., Ono H., Akamine S., Nishiyama K., Sanefuji M., Ishizaki Y., Torisu H., Saitsu H., Matsumoto N. and Hara T. (20161230). De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis. : BMC neurology.

MLA

Kanemasa Hikaru, Fukai Ryoko, Sakai Yasunari, Torio Michiko, Miyake Noriko, Lee Sooyoung, Ono Hiroaki, Akamine Satoshi, Nishiyama Kei, Sanefuji Masafumi, Ishizaki Yoshito, Torisu Hiroyuki, Saitsu Hirotomo, Matsumoto Naomichi and Hara Toshiro. De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis. : BMC neurology. 20161230.