Clinical features of codon 172 RDS macular dystrophy: Similar phenotype in 12 families

Archives of Ophthalmology

Volumn 117, Issue 10, 1999, Pages 1373-1383

  Downes, Susan M ^a,b   Fitzke, Frederick W ^b   Holder, Graham E ^a   Payne, Annette M ^b   Bessant, David A R ^a,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

ARGININE; DNA; GLUTAMINE;

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOFLUORESCENCE; CLINICAL FEATURE; CODON; ELECTRORETINOGRAPHY; EYE PHOTOGRAPHY; GENE; GENE MUTATION; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RETINA DEGENERATION; RETINA MACULA DEGENERATION; SCANNING LASER OPHTHALMOSCOPY; VISUAL ACUITY;

EID: 0033386160     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: 10.1001/archopht.117.10.1373     Document Type: Article

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