TY  - GEN
AU  - Kanemasa,Hikaru
AU  - Fukai,Ryoko
AU  - Sakai,Yasunari
AU  - Torio,Michiko
AU  - Miyake,Noriko
AU  - Lee,Sooyoung
AU  - Ono,Hiroaki
AU  - Akamine,Satoshi
AU  - Nishiyama,Kei
AU  - Sanefuji,Masafumi
AU  - Ishizaki,Yoshito
AU  - Torisu,Hiroyuki
AU  - Saitsu,Hirotomo
AU  - Matsumoto,Naomichi
AU  - Hara,Toshiro
TI  - De novo p.Arg756Cys mutation of ATP1A3 causes an atypical form of alternating hemiplegia of childhood with prolonged paralysis and choreoathetosis
SN  - 1471-2377
PY  - 2016///1230
KW  - Athetosis
KW  - complications
KW  - Child
KW  - Chorea
KW  - Hemiplegia
KW  - Humans
KW  - Male
KW  - Mutation
KW  - Paralysis
KW  - Phenotype
KW  - Sodium-Potassium-Exchanging ATPase
KW  - genetics
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1186/s12883-016-0680-6
ER  -