A missense mutation in SCN1A in brothers with severe myoclonic epilepsy in infancy (SMEI) inherited from a father with febrile seizures

• KIMURA Kazue

  Segawa Neurological Clinic for Children

• SUGAWARA Takashi

  Laboratory for Neurogenetics RIKEN Brain Science Institute

• MAZAKI-MIYAZAKI Emi

  Laboratory for Neurogenetics RIKEN Brain Science Institute

• HOSHINO Kyoko

  Segawa Neurological Clinic for Children

• NOMURA Yoshiko

  Segawa Neurological Clinic for Children

• TATENO Akihiko

  Department of Pediatrics, Toho University School of Medicine, Sakura Hospital

• HACHIMORI Kei

  Segawa Neurological Clinic for Children

• YAMAKAWA Kazuhiro

  Laboratory for Neurogenetics RIKEN Brain Science Institute

• SEGAWA Masaya

  Segawa Neurological Clinic for Children

収録刊行物

• Brain & development

  Brain & development 27 (6), 424-430, 2005-09-01

キーワード

• Severe myoclonic epilepsy in infancy (SMEI)
• Sodium channel
• SCN1A
• SCN2A

詳細情報

• CRID: 1573105975299882368
• NII論文ID: 10019356436
• NII書誌ID: AA00111153
• ISSN: 03877604
• Web Site: https://search.jamas.or.jp/link/ui/2006309115
• 本文言語コード: en
• データソース種別:
  • CiNii Articles