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

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Oral Presentation

genetic abnormality

[O17] Oral Presentation
teratology 3 -case report-

Fri. Jun 16, 2017 4:20 PM - 5:30 PM Room No.6 (10F Conference Room 1009)

Chair:Shinji Saitoh(Department of Pediatrics and Neonatology, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan), Shinsuke Ninomiya(Department of Clinical Genetics, Kurashiki Central Hospital, Okayama, Japan)

[O-103] TOE1 gene mutation cause pontocerebellar hypoplasia and disorders of sex development

○Tomomi Ogata1, Kazuhiro Muramatsu1, Noriko Sawaura1, Eriko Suzuki1, Hirokazu Arakawa1, Hirotomo Saitsu2, Naomichi Matsumoto3 (1.Department of Pediatrics,Gunma university Graduate School of Medicine,Maebashi, Japan, 2.Department of Biochemistry, Hamamatsu University School of medicine, Hamamatsu, Japan, 3.Department of Biochemistry,Yokohama City University Graduate School of Medicine, Yokohama,Japan)

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