Novel mutation of gene coding for glial fibrillary acidic protein in a Japanese patient with Alexander disease

• KAWAI Masanobu

  Department of Developmental Medicine (Pediatrics), D-5 Osaka University Graduate School of Medicine

• SAKAI Norio

  Department of Developmental Medicine (Pediatrics), D-5 Osaka University Graduate School of Medicine

• MIYAKE Susumu

  Kagawa Prefectural Central Hospital Dept of Pediatrics, Osaka University Graduate School of Medicine

• TSUKAMOTO Hiroko

  Department of Developmental Medicine (Pediatrics), D-5 Osaka University Graduate School of Medicine

• AKAGI Motohiro

  Department of Developmental Medicine (Pediatrics), D-5 Osaka University Graduate School of Medicine

• INUI Koji

  Department of Developmental Medicine (Pediatrics), D-5 Osaka University Graduate School of Medicine

• MUSHIAKE Sotaro

  Department of Developmental Medicine (Pediatrics), D-5 Osaka University Graduate School of Medicine

• TANIIKE Masako

  Department of Developmental Medicine (Pediatrics), D-5 Osaka University Graduate School of Medicine

• OZONO Keiichi

  Department of Developmental Medicine (Pediatrics), D-5 Osaka University Graduate School of Medicine

Journal

• Brain & development

  Brain & development 28 (1), 60-62, 2006-01

Keywords

• Alexander disease
• Glial fibrillary acidic protein
• Heterozygous mutation

Details

• CRID: 1570572700270331904
• NII Article ID: 10017319316
• NII Book ID: AA00111153
• ISSN: 03877604
• Web Site: https://search.jamas.or.jp/link/ui/2006310130
• Text Lang: en
• Data Source:
  • CiNii Articles