The 59th Annual Meeting of the Japanese Society of Child Neurology

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[O27] Oral Presentation
case report

Sat. Jun 17, 2017 10:40 AM - 11:50 AM Room No.6 (10F Conference Room 1009)

Chair:Reiko Arakawa(Institute of Medical Genetics, Tokyo Women's Medical University, Tokyo, Japan), Yukiko Kuroda( Department of Pediatrics, University of Tokyo, Tokyo, Japan)

[O-157] 3 Japanese CMT families with the mitofusin 2 (MFN2) mutations

○Shinobu Fukumura1, Shinobu Fukumura1, Akiyo Yamamoto1, Kentaro Kawamura1, Hiroyuki Tsutsumi1, Akiko Tsuduki2, Kouki Nikaido3, Akiko Yoshimura4, Akihiro Hashiguchi4, Hiroshi Takashima4 (1.The Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, Japan, 2.The Department of Rehabilitation, Hokkaido Medical Center for Child Health and Rehabilitation, Sapporo, Japan, 3.The Department of Child Neurology, Hokkaido Medical Center for Child Health and Rehabilitation, Sapporo, Japan, 4.The Department of Neurology and Geriatrics, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan)

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