Temporal macular thinning associated with X-linked alport syndrome

JAMA Ophthalmology

Volumn 131, Issue 6, 2013, Pages 777-782

  Ahmed, Faisal ^a   Kamae, Kandon K ^a   Jones, Denise J ^a   DeAngelis, Margaret M ^a   Hageman, Gregory S ^a   Gregory, Martin C ^b   Bernstein, Paul S ^a  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ALPORT SYNDROME; ARTICLE; CHILD; CLINICAL ARTICLE; DISEASE ASSOCIATION; DISEASE SEVERITY; EYE PHOTOGRAPHY; FEMALE; GENE EXPRESSION; GENE MUTATION; GENOTYPE; HUMAN; MALE; MEASUREMENT; OPTICAL COHERENCE TOMOGRAPHY; PRIORITY JOURNAL; RETINA MACULA LUTEA; RETINA MACULOPATHY; RETINAL THICKNESS; SCHOOL CHILD; TEMPORAL MACULAR THINNING;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CHILD; COLLAGEN TYPE IV; DIAGNOSTIC TECHNIQUES, OPHTHALMOLOGICAL; DISEASE PROGRESSION; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MACULA LUTEA; MACULAR DEGENERATION; MALE; MIDDLE AGED; MUTATION; NEPHRITIS, HEREDITARY; PHENOTYPE; PROGNOSIS; PROSPECTIVE STUDIES; RENAL INSUFFICIENCY; SEVERITY OF ILLNESS INDEX; TOMOGRAPHY, OPTICAL COHERENCE; UTAH; YOUNG ADULT;

EID: 84879035779     PISSN: 21686165     EISSN: None     Source Type: Journal    
DOI: 10.1001/jamaophthalmol.2013.1452     Document Type: Article

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