Clinical and molecular analysis of stargardt disease with preserved foveal structure and function

American Journal of Ophthalmology

Volumn 156, Issue 3, 2013, Pages

  Fujinami, Kaoru ^a,b,c,d   Sergouniotis, Panagiotis I ^a,b   Davidson, Alice E ^a,b   Wright, Genevieve ^a,b   Chana, Ravinder K ^a,b   Tsunoda, Kazushige ^c   Tsubota, Kazuo ^d   Egan, Catherine A ^a,b   Robson, Anthony G ^a,b   Moore, Anthony T ^a,b   Holder, Graham E ^a,b   Michaelides, Michel ^a,b   Webster, Andrew R ^a,b  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b MOORFIELDS EYE HOSPITAL   (United Kingdom)

^c NATIONAL HOSPITAL ORGANIZATION TOKYO MEDICAL CENTER   (Japan)

^d KEIO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ABCA4 GENE; ADULT; ARTICLE; AUTOFLUORESCENCE IMAGING; CASE STUDY; CENTRAL RETINAL THICKNESS; CLINICAL ARTICLE; CONTROLLED STUDY; ELECTROPHYSIOLOGY; EYE EXAMINATION; FEMALE; GENETIC VARIABILITY; HUMAN; HUMAN GENOME; MALE; MUTATIONAL ANALYSIS; ONSET AGE; OPTICAL COHERENCE TOMOGRAPHY; PHENOTYPE; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA FOVEA; RETINA MACULA DEGENERATION; RETROSPECTIVE STUDY; STARGARDT DISEASE; VISUAL ACUITY;

EID: 84882263713     PISSN: 00029394     EISSN: 18791891     Source Type: Journal    
DOI: 10.1016/j.ajo.2013.05.003     Document Type: Article

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