Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1

Archives of Ophthalmology

Volumn 119, Issue 1, 2001, Pages 96-105

  Downes, Susan M ^a,b   Holder, Graham E ^a   Fitzke, Frederick W ^b   Payne, Annette M ^b   Warren, Martin J ^b   Bhattacharya, Shomi S ^b   Bird, Alan C ^a,b  

^a MOORFIELDS EYE HOSPITAL   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

GUANYLATE CYCLASE ACTIVATING PROTEIN 1; GUANYLATE CYCLASE ACTIVATOR; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CLINICAL ARTICLE; DNA DETERMINATION; ELECTROPHYSIOLOGY; GENE MUTATION; HAPLOTYPE; HUMAN; MALE; OPHTHALMOSCOPY; PENETRANCE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PSYCHOPHYSIOLOGY; RETINA CONE; RETINA DYSTROPHY; RETINA ROD; SEX LINKAGE;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CALCIUM-BINDING PROTEINS; COLOR VISION DEFECTS; DNA; ELECTROOCULOGRAPHY; ELECTRORETINOGRAPHY; FEMALE; FLUORESCEIN ANGIOGRAPHY; GENES, DOMINANT; GUANYLATE CYCLASE; GUANYLATE CYCLASE-ACTIVATING PROTEINS; HUMANS; MALE; MIDDLE AGED; PEDIGREE; PHENOTYPE; PHOTORECEPTORS, VERTEBRATE; POINT MUTATION; RETINAL DEGENERATION; VISUAL ACUITY; VISUAL FIELDS;

EID: 0035139508     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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