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

• 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

Identity

PubMed Central ID

• PMC2868463

International Standard Serial Number (ISSN)

• 0146-0404

Digital Object Identifier (DOI)

• 10.1167/iovs.09-3585

PubMed ID

• 19741247

Additional Document Info

start page

• 1059

end page

• 1065

volume

• 51

issue

• 2