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[1P-406] Development of treatment method of Sandhoff disease mouse model that is one of lysosomal storage diseases

Kyoko Suzuki1, Akira Yamaguchi2, Shoji Yamanaka2, Makoto Kawashima2, Seiichi Kanzaki2, Noriko Koumitsu3, Mayumi Minamisawa4, Naoya Aoki1, Omi Katsuse1, Yoshio Hirayasu1 (1.Dept. of Psycho. Sch. of Med. The Univ. of Yokohama City, 2.Dept. Pathol. Sch. of Med. The Univ. of Yokohama City, 3.Dept. Dematol. Sch. of Med. The Univ. of Yokohama City, 4.Chiba Inst. Techno Univ.)

Sandhoff disease, ganglioside, autophagy, SOD2, synuclein

ksuzuki@yokohama-cu.ac.jp

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