Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin gene

• SHIONO T.

収録刊行物

• Jpn J Ophthalmol

  Jpn J Ophthalmol 36 69-75, 1992

詳細情報

• CRID: 1574231876425570176
• NII論文ID: 80006472020
• Web Site: https://search.jamas.or.jp/link/ui/1994118026
• データソース種別:
  • CiNii Articles