Phenotypic characteristics including in vivo cone photoreceptor mosaic in KCNV2-related "cone dystrophy with supernormal rod electroretinogram"

Investigative Ophthalmology and Visual Science

Volumn 54, Issue 1, 2013, Pages 898-908

  Vincent, Ajoy ^a,b   Wright, Tom ^a   Garcia Sanchez, Yaiza ^a   Kisilak, Marsha ^c   Campbell, Melanie ^c   Westall, Carol ^a,b   Héon, Elise ^a,b  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

^c UNIVERSITY OF WATERLOO   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; AUTOFLUORESCENCE IMAGING; CHILD; CLINICAL ARTICLE; COLOR VISION TEST; CONTRAST SENSITIVITY; CONTROLLED STUDY; ELECTRORETINOGRAPHY; FEMALE; FUNDUS CAMERA; GENE MUTATION; GENETIC SCREENING; HUMAN; MALE; MORPHOLOGICAL TRAIT; PERIMETRY; PHOTORECEPTOR; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RETINA CONE; RETINA MALFORMATION; SCANNING LASER OPHTHALMOSCOPY; SCHOOL CHILD; SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY; VISUAL IMPAIRMENT;

ADOLESCENT; CHILD; CODON, TERMINATOR; COLOR VISION; CONTRAST SENSITIVITY; DISEASE PROGRESSION; ELECTRORETINOGRAPHY; FEMALE; FRAMESHIFT MUTATION; HUMANS; LIPOFUSCIN; MALE; MOSAICISM; PHENOTYPE; PHOTIC STIMULATION; POTASSIUM CHANNELS, VOLTAGE-GATED; RETINAL CONE PHOTORECEPTOR CELLS; RETINAL ROD PHOTORECEPTOR CELLS; RETINITIS PIGMENTOSA; TOMOGRAPHY, OPTICAL COHERENCE;

EID: 84874705183     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.12-10971     Document Type: Article

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