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

Nature Genetics

Volumn 29, Issue 1, 2001, Pages 70-74

  Seeliger, Mathias W ^a   Grimm, Christian ^b   Ståhlberg, Fredrik ^a,c   Friedburg, Christoph ^a   Jaissle, Gesine ^a   Zrenner, Eberhart ^a   Guo, Hao ^a   Remé, Charlotte E ^b   Humphries, Peter ^d   Hofmann, Franz ^e   Biel, Martin ^f   Fariss, Robert N ^g   Redmond, T Michael ^g   Wenzel, Andreas ^b  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b UNIVERSITY HOSPITAL ZURICH   (Switzerland)

^c SWEDISH UNIVERSITY OF AGRICULTURAL SCIENCES   (Sweden)

^d TRINITY COLLEGE DUBLIN   (Ireland)

^e TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^f UNIVERSITY OF MUNICH   (Germany)

^g NATIONAL EYE INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN RPE65; UNCLASSIFIED DRUG;

ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHANNEL GATING; CONTROLLED STUDY; ELECTRORETINOGRAM; GENE MUTATION; GENETIC CODE; LEBER CONGENITAL AMAUROSIS; MOUSE; NONHUMAN; ONSET AGE; PRIORITY JOURNAL; PROTEIN DEFICIENCY; RETINA MALFORMATION; RETINA ROD; VISION;

ANIMALS; CARRIER PROTEINS; DISEASE MODELS, ANIMAL; ELECTRORETINOGRAPHY; EYE PROTEINS; MICE; MICE, MUTANT STRAINS; OPTIC ATROPHIES, HEREDITARY; PIGMENT EPITHELIUM OF EYE; PROTEINS; RODS (RETINA); VISION;

ANIMALIA;

EID: 17944379443     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng712     Document Type: Article

References (26)

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