Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese

Neurobiology of Aging - Tập 33 - Trang 1843.e19-1843.e24 - 2012
Aritoshi Iida1, Naoya Hosono2, Motoki Sano3, Tetsumasa Kamei4, Shuichi Oshima5, Torao Tokuda6, Masahiro Nakajima1, Michiaki Kubo2, Yusuke Nakamura7, Shiro Ikegawa1
1Laboratory for Bone and Joint Diseases, Center for Genomic Medicine, RIKEN, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108–8639, Japan
2Laboratory for Genotyping Development, Center for Genomic Medicine, RIKEN, 1-7-22 Suehiro-cho, Tsurumi-ku, Yokohama, Kanagawa 230–0045, Japan
3Department of Neurology, Chibanishi General Hospital, 107–1 Kanegasa-ku, Matsudo, Chiba 270–2251, Japan
4Department of Neurology, Chigasaki Tokushukai General Hospital, 14–1 Saiwai-cho, Chigasaki, Kanagawa 253–8558, Japan
5Department of Neurosurgery, Chiba Tokushukai Hospital, 1-27-1 Narashino-dai, Funabashi, Chiba 274–8503, Japan
6Tokushukai Group, 4-6-8 Kouji-Machi, Chiyoda-ku, Tokyo 102–0093, Japan
7Laboratory of Molecular Medicine, Human Genome Center, Institute of Medical Science, the University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108–8639, Japan

Tài liệu tham khảo

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Neurobiology of Aging

Tập 33

1843.e19-1843.e24

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