The 60th Annual Meeting of the Japanese Society of Child Neurology

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English Session

Hereditary disorder

[E3] English Session 3
Hereditary disorder

Fri. Jun 1, 2018 9:50 AM - 10:50 AM Room 8 (1F 103)

Chair:Mitsuhiro Kato（ Department of Pediatrics, Showa University School of Medicine,　Tokyo, Japan）,　Toshiyuki Yamamoto（ Institute of Medical Genetics, Tokyo Womens Medical University,　Tokyo, Japan）

[E-015] Paroxysmal dyskinetic disorders diagnosed by comprehensive genetic analysis.

Naoko Ishihara1, Misa Miyake1, Yoshiki Kawamura1, Hidehito Inagaki2, Takema Kato2, Makiko Tsutsumi2, Tadayoshi Hata3, Tetsushi Yoshikawa1, Hiroki Kurahashi2 (Department of Pediatrics, Fujita Health University School of Medicine, Toyoake, Japan1, Division of Molecular Genetics, Institute for Comprehensive Medical Science, Fujita Health University, Toyoake, Japan2, Faculty of Medical Technology, Fujita Health University School of Health Sciences, Toyoake, Japan3)

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