Ccdc66 null mutation causes retinal degeneration and dysfunction

Human Molecular Genetics

Volumn 20, Issue 18, 2011, Pages 3620-3631

  Gerding, Wanda M ^a   Schreiber, Sabrina ^a   Schulte Middelmann, Tobias ^a   Marques, Andreia de Castro ^b   Atorf, Jenny ^c   Akkad, Denis A ^a   Dekomien, Gabriele ^a   Kremers, Jan ^c   Dermietzel, Rolf ^a   Gal, Andreas ^d   Rülicke, Thomas ^e   Ibrahim, Saleh ^b   Epplen, Jörg T ^a   Petrasch Parwez, Elisabeth ^a  

^a RUHR UNIVERSITY BOCHUM   (Germany)

^b UNIVERSITY OF LÜBECK   (Germany)

^c UNIVERSITY HOSPITAL ERLANGEN   (Germany)

^d UNIVERSITY MEDICAL CENTER HAMBURG EPPENDORF   (Germany)

^e UNIVERSITY OF VETERINARY MEDICINE   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

MUTANT PROTEIN; PROTEIN CCDC66; RNA; UNCLASSIFIED DRUG;

AMPLITUDE MODULATION; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; CYTOLOGY; DISEASE COURSE; ELECTRON MICROSCOPY; ELECTRORETINOGRAPHY; FEMALE; GENE DISRUPTION; HUMAN; HUMAN TISSUE; MALE; MOUSE; NIGHT VISION; NONHUMAN; NUCLEOTIDE SEQUENCE; NULL ALLELE; PHOTOPIC VISION; PHOTORECEPTOR; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; RETINA CONE; RETINA DEGENERATION; RETINA DISEASE; RETINA MALFORMATION; RETINA ROD OUTER SEGMENT; RETINAL DYSFUNCTION; WILD TYPE;

ANIMALS; DISEASE MODELS, ANIMAL; EYE PROTEINS; FEMALE; GENE SILENCING; HUMANS; MALE; MICE; MICE, KNOCKOUT; RETINA; RETINAL DEGENERATION; RETINITIS PIGMENTOSA; SEQUENCE DELETION;

CANIS FAMILIARIS; MURINAE; MUS;

EID: 80052237572     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddr282     Document Type: Article

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