IDENTIFICATION OF ATP1A3 MUTATIONS BY EXOME SEQUENCING AS THE CAUSE OF ALTERNATING HEMIPLEGIA OF CHILDHOOD IN JAPAN

被引：0

作者：

Ishii, A. ^{[1
]}

Saito, Y. ^{[2
]}

Mitsui, J. ^{[3
]}

Ishiura, H. ^{[3
]}

Yoshimura, J. ^{[4
]}

Arai, H. ^{[5
]}

Yamashita, S. ^{[6
]}

Kimura, S. ^{[7
,8
]}

Oguni, H. ^{[9
]}

Morishita, S. ^{[4
]}

Tsuji, S. ^{[3
]}

Sasaki, M. ^{[2
]}

Hirose, S. ^{[1
]}

机构：

[1] Fukuoka Univ, Sch Med, Dept Pediat, Fukuoka 81401, Japan

[2] Natl Ctr Neurol & Psychiat, Dept Child Neurol, Kodaira, Tokyo, Japan

[3] Univ Tokyo, Grad Sch Med, Dept Neurol, Tokyo, Japan

[4] Univ Tokyo, Grad Sch Frontier Sci, Dept Computat Biol, Kashiwa, Chiba, Japan

[5] Chiba Childrens Hosp, Dept Neurol, Chiba, Japan

[6] Kanagawa Childrens Med Ctr, Div Child Neurol, Yokohama, Kanagawa, Japan

[7] Osaka Med Ctr, Div Child Neurol, Izumi, Japan

[8] Res Inst Maternal & Child Hlth, Izumi, Japan

[9] Tokyo Womens Med Univ, Dept Pediat, Tokyo, Japan

来源：

EPILEPSIA | 2013年 / 54卷

关键词：

D O I：

暂无

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：295 / 295

页数：1

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