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

Presentation information

Oral Presentation

Hereditary disorder/Chromosomal aberration

[O19] Hereditary disorder/Chromosomal aberration

Fri. Jun 1, 2018 11:00 AM - 11:50 AM Room 7 (3F 304)

Chair:Takahito WADA(Kyoto University Graduate School of Medicine, Department of Medical Ethics and Medical Genetics), Nobuyuki Murakami(Dokkyo Medical University, Saitama Medical Center, Department of Pediatrics)

[O-101] Two boys of episodic ataxia type 2 with epilepsy due to a mutation in CACNA1A

Ken Nakajima1, RIE NAKAI1, taikan Oboshi1, YUICHI KIMIZU1, TAE IKEDA1, YUKIKO MOGAMI1, KEIKO YANAGIHARA1, NOBUHIKO OKAMOTO2, AKIHIRO YASUHARA3, YASUHIRO SUZUKI1 (1.Department of Pediatric Neurology,Osaka Women's and children's Hospital,Osaka,Japan, 2.Department of Medical Genetics,Osaka Women's and children's Hospital,Osaka,Japan)

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