Presentation Information
[O18-1]Whole-exome sequencing reveals the genetic causes and modifiers of moyamoya syndrome
○Hiroyuki Akagawa1,2,3, Akikazu Nakamura1,4, Shunsuke Nomura5, Shoko Hara6, Thiparpa Thamamongood6, Kay Sin Tan7, Constantin Roder8, Takakazu Kawamata4 (1.Institute for Comprehensive Medical Sciences, Tokyo Women's Medical University, Tokyo, Japan, 2.Department of Neurosurgery, Adachi Medical Center, Tokyo Women's Medical University, Tokyo, Japan, 3.Medical AI Center, Tokyo Women's Medical University, Tokyo, Japan, 4.Department of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan, 5.Krembil Brain Institute, University of Toronto, Canada, 6.Department of Neurosurgery, Tokyo Medical and Dental University, Tokyo, Japan, 7.Department of Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia, 8.Department of Neurosurgery, Eberhard Karls University Tubingen, Tubingen, Germany)