Lrit3 deficient mouse (nob6): A novel model of complete congenital stationary night blindness (cCSNB)

PLoS ONE

Volumn 9, Issue 3, 2014, Pages

  Neuillé, Marion ^a,b,c   El Shamieh, Said ^a,b,c   Orhan, Elise ^a,b,c   Michiels, Christelle ^a,b,c   Antonio, Aline ^a,b,c,d   Lancelot, Marie Elise ^a,b,c   Condroyer, Christel ^a,b,c   Bujakowska, Kinga ^a,b,c,e   Poch, Olivier ^b   Sahel, José Alain ^{a,b,c,d,f,g,h}   Audo, Isabelle ^a,b,c,d,f   Zeitz, Christina ^a,b,c  

^a INSERM   (France)

^b CNRS   (France)

^c SORBONNE UNIVERSITÉ   (France)

^d CENTRE HOSPITALIER NATIONAL D OPHTALMOLOGIE DES QUINZE VINGTS   (France)

^e MASSACHUSETTS EYE AND EAR INFIRMARY   (United States)

^f UNIVERSITY COLLEGE LONDON   (United Kingdom)

^g FONDATION OPHTALMOLOGIQUE ADOLPHE DE ROTHSCHILD   (France)

^h Académie des Sciences Institut de France Paris   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; AUTOFLUORESCENCE; CONGENITAL STATIONARY NIGHT BLINDNESS; CONTROLLED STUDY; DARK ADAPTATION; DISEASE MODEL; ELECTRORETINOGRAM; EYE EXAMINATION; EYE FUNDUS; FEMALE; GENE; GENE CASSETTE; GENE MUTATION; GENETIC CODE; HISTOLOGY; LRIT3 GENE; MALE; MOUSE; NIGHT BLINDNESS; NONHUMAN; NUCLEOTIDE SEQUENCE; OPTICAL COHERENCE TOMOGRAPHY; OPTOMOTOR TEST; PHENOTYPE; RETINA; SIGNAL TRANSDUCTION; 129 MOUSE; AMINO ACID SEQUENCE; ANIMAL; C57BL MOUSE; DEFICIENCY; EYE DISEASE; EYE MOVEMENT; GENETICS; HEAD MOVEMENT; KNOCKOUT MOUSE; MOLECULAR GENETICS; MYOPIA; PATHOLOGY; PATHOPHYSIOLOGY; X CHROMOSOME LINKED DISORDER;

LRIT3 PROTEIN, MOUSE; MEMBRANE PROTEIN;

AMINO ACID SEQUENCE; ANIMALS; DISEASE MODELS, ANIMAL; EYE DISEASES, HEREDITARY; EYE MOVEMENTS; FEMALE; GENETIC DISEASES, X-LINKED; HEAD MOVEMENTS; MALE; MEMBRANE PROTEINS; MICE, 129 STRAIN; MICE, INBRED C57BL; MICE, KNOCKOUT; MOLECULAR SEQUENCE DATA; MYOPIA; NIGHT BLINDNESS; RETINA;

EID: 84897146248     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0090342     Document Type: Article

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