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J-GLOBAL ID：201902214563961863   Reference number：19S1267981

Molecular impairment mechanisms of novel OPA1 mutations predicted by molecular modeling in patients with autosomal dominant optic atrophy and auditory neuropathy spectrum disorder

Author (12)： Namba, Kazunori (Laboratory of Auditory Disorders, National Institute of Sensory Organs, National Tokyo Medical Center) ,  Mutai, Hideki (Laboratory of Auditory Disorders, National Institute of Sensory Organs, National Tokyo Medical Center) ,  Matsunaga, Tatsuo (Laboratory of Auditory Disorders, National Institute of Sensory Organs, National Tokyo Medical Center) ,  Takiguchi, Yoichiro (Department of Otolaryngology, Eiju General Hospital) ,  Yagi, Hirotaka (1st Government and Public Solutions Division, NEC Solution Innovators, Ltd) ,  Okuyama, Takahide (Graduate School of Integrated Basic Sciences, Nihon University) ,  Kaneko, Hiroki (Graduate School of Integrated Basic Sciences, Nihon University) ,  Kaneko, Hiroki (Department of Integrated Science in Physics and Biology, College of Humanities and Science, Nihon University) ,  Oba, Shuntaro (Department of Integrated Science in Physics and Biology, College of Humanities and Science, Nihon University) ,  Yamagishi, Ryosuke (Department of Integrated Science in Physics and Biology, College of Humanities and Science, Nihon University) ,  Shintani, Tomoko (Department of Otolaryngology, Sapporo Medical University School of Medicine) ,  Kaga, Kimitaka (National Institute of Sensory Organs, National Tokyo Medical Center)
Material： Otology and Neurotology
Volume： 37  Issue： 4  Page： 394-402  Publication year： 2016 
JST Material Number： SCOPUS  ISSN： 1531-7129  CODEN： ONTEA 
Country of issue： United States (USA)  Language： English (EN)

Terms in the title (1)： OPA1