[1P-305] Functional impacts of pathological mutations in IP3 receptor type I identified in spinocerebellar ataxia 29

^○Hideaki Ando^1,2, Matsumi Hirose^1,3, Katsuhiko Mikoshiba^1,4 (1.Laboratory for Developmental Neurobiology, Center for Brain Science, RIKEN, 2.Laboratory of Molecular Biomedicine for Pathogenesis, Faculty of Medicine, The University of Tokyo, 3.Collaborative Research Resources, School of Medicine, Keio University, 4.Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University)

キーテクノロジー：カルシウムイメージング

カルシウム、IP3受容体、神経変性疾患、遺伝性疾患、CA8