The 60th Annual Meeting of the Japanese Society of Child Neurology

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English Session

Hereditary disorder

[E3] English Session 3
Hereditary disorder

Fri. Jun 1, 2018 9:50 AM - 10:50 AM Room 8 (1F 103)

Chair:Mitsuhiro Kato（ Department of Pediatrics, Showa University School of Medicine,　Tokyo, Japan）,　Toshiyuki Yamamoto（ Institute of Medical Genetics, Tokyo Womens Medical University,　Tokyo, Japan）

[E-016] Utility of single—fiber electromyography in patients with CACNA1A mutation

Ayaka Hirasawa1, Akihiko Ishiyama1, Eri Takeshita1, Yuko Shimizu—motohashi1, Takashi Saito1, Hirofumi Komaki1, Eiji Nakagawa1, Kenji Sugai1, Shota Yuasa2, Kohei Hamanaka3, Satoko Miyatake3, Naomichi Matsumoto3, Masayuki Sasaki1 (Department of Child Neurology, National Center Hospital, National Center of Neurology and Psychiatry（NCNP）, Tokyo, Japan1, Department of Pediatrics, Kameda Medical Center, Chiba, Japan2, Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan3)

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