LABORATORY INVESTIGATION : OPA1 mutations in Japanese patients suspected to have autosomal dominant optic atrophy

• Tetsuya Hamahata

• Takuro Fujimaki

• Keiko Fujiki

収録刊行物

• Japanese journal of ophthalmology : the official international journal of the Japanese Ophthalmological Society / Japanese Ophthalmological Society

  Japanese journal of ophthalmology : the official international journal of the Japanese Ophthalmological Society / Japanese Ophthalmological Society 56 (1), 91-97, 2012

  [Tokyo] : Springer

キーワード

• OPA1
• Autosomal dominant optic atrophy
• Mitochondria
• Mutation

詳細情報

• CRID: 1520854803540869376
• NII論文ID: 10030248522
• NII書誌ID: AA00691177
• ISSN: 00215155
• NDL書誌ID: 023385941
• Web Site: https://ndlsearch.ndl.go.jp/books/R000000004-I023385941
• Web Site: https://search.jamas.or.jp/link/ui/2013077842
• 本文言語コード: en
• NDL 雑誌分類:
  • ZS42(科学技術--医学--眼科学)
• データソース種別:
  • NDL
  • CiNii Articles