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

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English Session

genetic abnormality

[E5] English Session 5
genetic disorder

Fri. Jun 16, 2017 8:50 AM - 9:50 AM Room No.6 (10F Conference Room 1009)

Chair:Yoshiko Nomura（Yoshiko Nomura Neurological Clinic for Children, Tokyo, Japan）, Toshiyuki Yamamoto（Institute of Medical Genetics, Tokyo Women’s Medical University, Tokyo, Japan）

[E-033] SZT2 mutations cause a discernible disorder with developmental delay and dysmorphic corpus callosum

○Yuji Nakamura1, Yasuko Togawa2, Yusuke Okuno3, Hideki Muramatsu3, Daisuke Ieda1, Ikumi Hori1, Yutaka Negishi1, Ayako Hattori1, Shinji Saitoh1 (1.Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan, 2.Department of Pediatrics, Toyohashi Municipal Hospital, Aichi, Japan, 3.Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan)

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