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De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis. [electronic resource] by
- 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
- Hara, Toshiro
Producer: 20161230
In:
BMC neurology vol. 16
Availability: No items available.
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