Screening and detection of gene mutations in Japanese patients with Fabry disease by non-radioactive single-stranded conformation polymorphism analysis

• TAKATA Tomoyo

  Department of Clinical Genetics,The Tokyo Metropolitan Institute of Medical Science,School of Allied Health Sciences,Faculty of Medicine,Tokyo Medical and Dental University

• OKUMIYA Toshika

  Department of Clinical Genetics,The Tokyo Metropolitan Institute of Medical Science,School of Allied Health Sciences,Faculty of Medicine,Tokyo Medical and Dental University

• HAYASHIBE Hidemasa

  Department of Clinical Genetics,The Tokyo Metropolitan Institute of Medical Science,Department of Pediatrics,Yamanashi Medical College

• SHIMMOTO Michie

  Department of Clinical Genetics,The Tokyo Metropolitan Institute of Medical Science

• KASE Ryoichi

  Department of Clinical Genetics,The Tokyo Metropolitan Institute of Medical Science

• ITOH Kohji

  Department of Clinical Genetics,The Tokyo Metropolitan Institute of Medical Science

• UTSUMI Koichi

  Department of Clinical Genetics,The Tokyo Metropolitan Institute of Medical Science,The Second Department of Internal Medicine,Nippon Medical School,Department of Internal Medicine,Kasukabe Shuei Hospital

• KAMEI Sachiko

  School of Allied Health Sciences,Faculty of Medicine,Tokyo Medical and Dental University

• SAKURABA Hitoshi

  Department of Clinical Genetics,The Tokyo Metropolitan Institute of Medical Science

収録刊行物

• Brain & development

  Brain & development 19 (2), 111-116, 1997

キーワード

• Fabry disease
• α-Galactosidase
• Polymerase chain reaction
• Single-stranded conformation polymorphism
• Gene diagnosis

詳細情報

• CRID: 1573950399249011072
• NII論文ID: 10006194150
• NII書誌ID: AA00111153
• ISSN: 03877604
• Web Site: https://search.jamas.or.jp/link/ui/1997212525
• 本文言語コード: en
• データソース種別:
  • CiNii Articles