[1P] Neurodegenerative Disorders

[1P-217] Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia

*Yui Tada¹, Kodai Kume¹, Yukiko Matsuda¹, Takashi Kurashige², Yuhei Kanaya¹, Ryosuke Ohsawa¹, Hiroyuki Morino¹, Hayato Tabu³, Satoshi Kaneko⁴, Toshihiko Suenaga⁵, Akira Kakizuka⁶, Hideshi Kawakami¹ (1.Department of Epidemiology Research Institute for Radiology and Medicine Hiroshima University, 2.Department of Neurology, National Hospital Organization Kure Medical Center and Chugoku Cancer Center, Kure, Japan, 3.Department of Neurology, Kitano Hospital, Osaka, Japan, 4.Department of Neurology, Kansai Medical University, Osaka, Japan, 5.Department of Neurology, Tenri Hospital, Tenri, Japan, 6.Laboratory of Functional Biology, Graduate School of Biostudies, Kyoto University, Kyoto, Japan)