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Severe retinal degeneration caused by a novel rhodopsin mutation

Academic Article
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Overview

authors

  • Liu, H. Q.
  • Wang, M.
  • Xia, C. H.
  • Du, X.
  • Flannery, J. G.
  • Ridge, K. D.
  • Beutler, Bruce
  • Gong, Xiaohua

publication date

  • February 2010

journal

  • Investigative Ophthalmology & Visual Science  Journal

subject areas

  • Animals
  • Base Sequence
  • Blotting, Western
  • DNA Mutational Analysis
  • Electroretinography
  • Ethylnitrosourea
  • Genes, Dominant
  • Genome-Wide Association Study
  • Immunohistochemistry
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mice, Mutant Strains
  • Molecular Sequence Data
  • Mutagenesis
  • Ophthalmoscopy
  • Phenotype
  • Photoreceptor Cells, Vertebrate
  • Point Mutation
  • Protein Structure, Secondary
  • Retinal Degeneration
  • Rhodopsin
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Identity

PubMed Central ID

  • PMC2868463

International Standard Serial Number (ISSN)

  • 0146-0404

Digital Object Identifier (DOI)

  • 10.1167/iovs.09-3585

PubMed ID

  • 19741247
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Additional Document Info

start page

  • 1059

end page

  • 1065

volume

  • 51

issue

  • 2

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