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

Presentation information

Oral Presentation

other

[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-158] A case with novel complex heterozygous mutation within PCDH12 gene.

Sato Suzuki-muromoto1, Takuya Miyabayashi1, Yusuke Takezawa2, Yukimune Ookubo1, Wakaba Endou1, Takehiko Inui1, Keisuke Wakusawa1, Noriko Togashi1, Kazuhiro Haginoya1, Mitsuko Nakashima3, Hirotomo Saitsu4, Naomichi Matsumoto3 (1.Department of Pediatric Neurology, Miyagi Childrens Hospital, Sendai, Japan, 2.Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan, 3.Department of Human Genetics, Yokohama City University,Yokohama, Japan, 4.Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan)

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