De novo p.Arg756Cys mutation of ATP1A3 causes an atypical...

BMC Neurology 2016 / 12 Vol. 16; Iss. 1

De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis

Kanemasa, Hikaru, Fukai, Ryoko, Sakai, Yasunari, Torio, Michiko, Miyake, Noriko, Lee, Sooyoung, Ono, Hiroaki, Akamine, Satoshi, Nishiyama, Kei, Sanefuji, Masafumi, Ishizaki, Yoshito, Torisu, Hiroyuki,
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Volume:
16
Language:
english
Journal:
BMC Neurology
DOI:
10.1186/s12883-016-0680-6
Date:
December, 2016
File:
PDF, 1022 KB
english, 2016
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