SLC2A1 gene analysis of Japanese patients with glucose transporter 1 deficiency syndrome

• HASHIMOTO Natsuko

  Department of Pediatrics, Osaka University Graduate School of Medicine

• KAGITANI SHIMONO Kuriko

  Department of Pediatrics, Osaka University Graduate School of Medicine

• SAKAI Norio

  Department of Pediatrics, Osaka University Graduate School of Medicine

• OTOMO Takanobu

  Department of Pediatrics, Osaka University Graduate School of Medicine

• TOMINAGA Koji

  Department of Pediatrics, Osaka University Graduate School of Medicine

• NABATAME Shin

  Department of Pediatrics, Osaka University Graduate School of Medicine

• MOGAMI Yukiko

  National Epilepsy Center, Shizuoka Institute of Epilepsy and Neurological Disorders

• TAKAHASHI Yukitoshi

  National Epilepsy Center, Shizuoka Institute of Epilepsy and Neurological Disorders

• IMAI Katsumi

  National Epilepsy Center, Shizuoka Institute of Epilepsy and Neurological Disorders

• YANAGIHARA Keiko

  Osaka Medical Center and Research Institute for Maternal and Child Health

• OKINAGA Takeshi

  Department of Pediatrics, Osaka University Graduate School of Medicine

• NAGAI Toshisaburo

  Division of Health Sciences, Osaka University Graduate School of Medicine

• TANIIKE Masako

  United Graduate School of Child Development, Osaka University Graduate School of Medicine

• OZONO Keiichi

  Department of Pediatrics, Osaka University Graduate School of Medicine

収録刊行物

• Journal of human genetics

  Journal of human genetics 56 (12), 846-851, 2011-12-01

キーワード

• glucose transporter 1 deficiency syndrome
• mutation
• SLC2A1

詳細情報

• CRID: 1572543025654372480
• NII論文ID: 10030661947
• NII書誌ID: AA11206160
• ISSN: 14345161
• 本文言語コード: en
• データソース種別:
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