Fundus autofluorescence in carriers of X-linked recessive retinitis pigmentosa associated with mutations in RPGR, and correlation with electrophysiological and psychophysical data

Graefe's Archive for Clinical and Experimental Ophthalmology

Volumn 242, Issue 6, 2004, Pages 501-511

  Wegscheider, Erika ^a   Preising, Markus N ^a   Lorenz, Birgit ^a  

^a UNIVERSITY OF REGENSBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; PROTEIN RPGR; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGED; ARTICLE; AUTOFLUORESCENCE; CHILD; CLINICAL ARTICLE; CLINICAL EXAMINATION; CONTROLLED STUDY; CORRELATION FUNCTION; DATA ANALYSIS; DIAGNOSTIC TEST; DISEASE ASSOCIATION; ELECTRORETINOGRAPHY; EMBRYO DEVELOPMENT; EYE FUNDUS; EYE PHOTOGRAPHY; FAMILY STUDY; GENE MUTATION; HETEROZYGOTE; HUMAN; INTERMETHOD COMPARISON; KINETICS; OPHTHALMOSCOPY; PERIMETRY; PRIORITY JOURNAL; PSYCHOPHYSIOLOGY; RANDOMIZATION; RETINA CONE; RETINA DEVELOPMENT; RETINA ROD; RETINITIS PIGMENTOSA; SENSITIVITY ANALYSIS; SENSORY SYSTEM ELECTROPHYSIOLOGY; X CHROMOSOME INACTIVATION; X CHROMOSOME RECESSIVE DISORDER;

EID: 3543044979     PISSN: 0721832X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00417-004-0891-1     Document Type: Article

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