New views on RPE65 deficiency: the rod system is the source of vision in a mouse model of Leber congenital amaurosis.

Seeliger, M W; Grimm, C; Ståhlberg, F; Friedburg, C; Jaissle, G; Zrenner, E; Guo, H; Remé, C E; Humphries, P; Hofmann, F; Biel, M; Fariss, R N; Redmond, T M; Wenzel, A

Seeliger, M W; Grimm, C; Ståhlberg, F; Friedburg, C; Jaissle, G; Zrenner, E; Guo, H; Remé, C E; Humphries, P; Hofmann, F; Biel, M; Fariss, R N; Redmond, T M; Wenzel, A.

Affiliation

Seeliger MW; Retinal Electrodiagnostics Research Group, Department of Ophthalmology, University of Tübingen, Germany. see@uni-tuebingen.de

Nat Genet ; 29(1): 70-4, 2001 Sep.

Article in En | MEDLINE | ID: mdl-11528395

Subject(s)

Optic Atrophies, Hereditary/genetics; Pigment Epithelium of Eye/physiology; Proteins/genetics; Retinal Rod Photoreceptor Cells/physiopathology; Vision, Ocular/physiology; Animals; Carrier Proteins; Disease Models, Animal; Electroretinography; Eye Proteins; Mice; Mice, Mutant Strains; Optic Atrophies, Hereditary/physiopathology; cis-trans-Isomerases

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Collection: 01-internacional Database: MEDLINE Main subject: Pigment Epithelium of Eye / Vision, Ocular / Proteins / Optic Atrophies, Hereditary / Retinal Rod Photoreceptor Cells Limits: Animals Language: En Journal: Nat Genet Journal subject: GENETICA MEDICA Year: 2001 Type: Article Affiliation country: Germany

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