Art
J-GLOBAL ID:200902181305463619   Reference number:02A0876907

Electroretinographic Findings in Three Family Members with X-linked Juvenile Retinoschisis Associated with a Novel Pro192Thr Mutation of the XLRS1 Gene.

XLRS1遺伝子の異常なPro192Thr変異が関連したX染色体連関若年性網膜分離症の3家族の網膜電図所見
Author (8):
Material:
Volume: 46  Issue:Page: 568-576  Publication year: Sep. 2002 
JST Material Number: W0991A  ISSN: 0021-5155  Document type: Article
Article type: 原著論文  Country of issue: United States (USA)  Language: ENGLISH (EN)
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JST classification (2):
JST classification
Category name(code) classified by JST.
Eye diagnosis(= ophthalmic diagnosis)  ,  Diagnostics of congenital diseases, deformities. 
Reference (38):
  • HAAS, J. Ueber das Zusammenvorkommen von Veranderungen der Retina und Choroidea. Arch Augenheilkd. 1898, 37, 343-348
  • YANOFF, M. Histopathology of juvenile retinoschisis. Arch Ophthalmol. 1968, 79, 49-53
  • BROCKHURST, RJ. Photocoagulation in congenital retinoschisis. Arch Ophthalmol. 1970, 84, 158-165
  • DEUTMAN, AF. Sex-linked juvenile retinoschisis. Hereditary dystrophies of the posterior pole of the eye. 1971, 48-99
  • PROSPERI, L. Congenital hereditary sex-linked retinoschisis. J Pediatr Ophthalmol Strabismus. 1978, 15, 26-30
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