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J-GLOBAL ID:202002244555565805   Reference number:20A0739868

Investigations of Gene Pathogenicity and Establishment of a Patient Data Bank for the Hereditary Chorioretinal Dystrophy

網脈絡膜ジストロフィの遺伝学的病態解明および治療に向けた症例データバンクの構築
Author (14):
Material:
Volume: 124  Issue:Page: 247-283  Publication year: Mar. 10, 2020 
JST Material Number: Z0666A  ISSN: 0029-0203  Document type: Article
Article type: 文献レビュー  Country of issue: Japan (JPN)  Language: JAPANESE (JA)
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JST classification (3):
JST classification
Category name(code) classified by JST.
Eye diseases  ,  Congenital diseases,deformities in general.  ,  Medical information processing 
Reference (108):
  • Jiang DJ, Xu CL, Tsang SH : Revolution in gene medicine therapy and genome surgery. Genes (Basel) 9 : 575, 2018.
  • Berger W, Kloeckener-Gruissem B, Neidhardt J : The molecular basis of human retinal and vitreoretinal diseases. Prog Retin Eye Res 29 : 335-375, 2010.
  • Audo I, Bujakowska KM, Léveillard T, Mohand-Saïd S, Lancelot ME, Germain A, et al : Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases. Orphanet J Rare Dis 7 : 8, 2012.
  • Neveling K, Collin RW, Gilissen C, van Huet RA, Visser L, Kwint MP, et al : Next-generation genetic testing for retinitis pigmentosa. Hum Mutat 33 : 963-972, 2012.
  • Roosing S, Thiadens AA, Hoyng CB, Klaver CC, den Hollander AI, Cremers FP : Causes and consequences of inherited cone disorders. Prog Retin Eye Res 42 : 1-26, 2014.
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