The Molecular Biology Society of Japan

The 42nd Annual Meeting of the Molecular Biology Society of Japan

The 42nd Annual Meeting of the Molecular Biology Society of Japan

Dec 3, 2019 - Dec 6, 2019
Fukuoka International Congress Center・Fukuoka sunpalace hotel & hall・Marine Messe Fukuoka

[2P-0446] Characterization of pathological mutations in IP3 receptor type I and CA8 identified in hereditary ataxia

〇Hideaki Ando1,2, Matsumi Hirose1,3, Katsuhiko Mikoshiba1,4 (1.Lab. for Dev. Neurobiol., CBS, RIKEN, 2.Lab. of Mol. Biomed. for Pathog., Facul. of Med., Univ. of Tokyo, 3.Collab. Res. Resources, Sch. of Med, Keio Univ., 4.SIAIS, ShanghaiTech Univ.)

spinocerebellar ataxia, IP3 receptor, CA8, calcium signaling, hereditary ataxia

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