Oligocone trichromacy is part of the spectrum of CNGA3-related cone system disorders

Ophthalmic Genetics

Volumn 32, Issue 2, 2011, Pages 107-113

  Vincent, Ajoy ^a   Wright, Tom ^a   Billingsley, Gail ^a   Westall, Carol ^a,b   Héon, Elise ^a,b  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

^b UNIVERSITY OF TORONTO   (Canada)

Author keywords

achromatopsia; bradyopsia; CNGA3 protein, human; CNGB3 protein, human; color vision defects; cyclic Nucleotide Gated Cation Channels; electroretinography; oligocone trichromacy

Indexed keywords

CYCLIC NUCLEOTIDE GATED CHANNEL;

ADULT; ARTICLE; CASE REPORT; CNGA3 GENE; CNGB3 GENE; COLOR VISION; COLOR VISION DEFECT; COLOR VISION TEST; DNA SEQUENCE; ELECTRORETINOGRAM; GENE; GENE MUTATION; HUMAN; MALE; OLIGOCONE TRICHROMACY; OPTICAL COHERENCE TOMOGRAPHY; PERIMETRY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RETINA CONE; VISUAL ACUITY;

AMINO ACID SEQUENCE; BASE SEQUENCE; COLOR PERCEPTION TESTS; COLOR VISION DEFECTS; CYCLIC NUCLEOTIDE-GATED CATION CHANNELS; DNA MUTATIONAL ANALYSIS; ELECTRORETINOGRAPHY; FLUORESCEIN ANGIOGRAPHY; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; PHENOTYPE; POLYMERASE CHAIN REACTION; RETINAL CONE PHOTORECEPTOR CELLS; RETINAL DISEASES; TOMOGRAPHY, OPTICAL COHERENCE; VISUAL FIELDS; YOUNG ADULT;

EID: 79955827261     PISSN: 13816810     EISSN: 17445094     Source Type: Journal    
DOI: 10.3109/13816810.2010.544366     Document Type: Article

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