Presentation Information

[O10-05]Mitochondrial Dysfunction in Digenic TBP/STUB1 Spinocerebellar Ataxia

Kazuki Yamada1,2, Shunsuke Ogata1,3, Satoko Miyatake1,4, Hisashi Uwatoko2, Shinichi Shirai2, Eriko Koshimizu1, Kohei Hamanaka1, Naomi Tsuchida1,5, Yuri Uchiyama1,5, Masamune Sakamoto1, Takeshi Mizuguchi1, Ichiro Yabe2, Naomichi Matsumoto1,4,5 (1. Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan, 2. Department of Neurology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan, 3. Department of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan, 4. Department of Clinical Genetics, Yokohama City University Hospital, Yokohama, Japan, 5. Department of Rare Disease Genomics, Yokohama City University Hospital, Yokohama, Japan)

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