High-resolution optical coherence tomography imaging in KCNV2 retinopathy

British Journal of Ophthalmology

Volumn 96, Issue 2, 2012, Pages 213-217

  Sergouniotis, Panagiotis I ^a,b   Holder, Graham E ^a   Robson, Anthony G ^a   Michaelides, Michel ^a,b   Webster, Andrew R ^a,b   Moore, Anthony T ^a,b  

^a MOORFIELDS EYE HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

ADOLESCENT; ADULT; AMINO ACID SUBSTITUTION; ARTICLE; AUTOFLUORESCENCE IMAGING; CLINICAL ARTICLE; COLOR VISION TEST; CONTROLLED STUDY; ELECTRORETINOGRAM; EYE REFRACTION; FRAMESHIFT MUTATION; GENE; GENE DELETION; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; KCNV2 GENE; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; OPHTHALMOSCOPY; PHENOTYPE; PHOTOPHOBIA; PHOTORECEPTOR INNER SEGMENT; PHOTORECEPTOR OUTER SEGMENT; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA FOVEA; RETINA THICKNESS; RETINOPATHY; SPECTRAL DOMAIN OPTICAL COHERENCE TOMOGRAPHY; VISUAL ACUITY; VISUAL DISORDER; VISUAL SYSTEM PARAMETERS;

ADOLESCENT; ADULT; DARK ADAPTATION; ELECTRORETINOGRAPHY; FLUORESCEIN ANGIOGRAPHY; HUMANS; MIDDLE AGED; MUTATION; PHOTIC STIMULATION; POTASSIUM CHANNELS, VOLTAGE-GATED; RETINAL CONE PHOTORECEPTOR CELLS; RETINAL DYSTROPHIES; SIBLINGS; TOMOGRAPHY, OPTICAL COHERENCE; YOUNG ADULT;

EID: 84856030990     PISSN: 00071161     EISSN: 14682079     Source Type: Journal    
DOI: 10.1136/bjo.2011.203638     Document Type: Article

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