Presentation Information

[1P-722]Functional and structural analysis of the RAC3 p.N92K mutation implicated in neurodevelopmental disorders

○Keisuke Hamada1, Ryota Sugawara 2,3, Hidenori Ito 2, Marcello Scala 4,5, Hiroshi Ueda 3,6, Hidenori Tabata 2, Koh-ichi Nagata 2,7, Kazuhiro Ogata 1,8 (1. Dept. of Biochemistry, Yokohama City Univ. Grad. Sch. Med., 2. Dept. of Molecular Neurobiology, Inst. for Developmental Research, Aichi Dev. Disability Center, 3. United Grad. Sch. of Drug Discovery & Med. Info. Sci., Gifu Univ., 4. Dept. of Neurosciences, Univ. of Genoa, 5. Unit of Medical Genetics, IRCCS Giannina Gaslini Inst., 6. Center for One Medicine Innovative Translational Research (COMIT), Gifu Univ., 7. Dept. of Neurochemistry, Nagoya Univ. Grad. Sch. Med., 8. Grad. Sch., Int. Univ. of Health and Welfare)

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