Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations

Investigative Ophthalmology and Visual Science

Volumn 48, Issue 10, 2007, Pages 4759-4765

  Aleman, Tomas S ^a   Cideciyan, Artur V ^a   Sumaroka, Alexander ^a   Schwartz, Sharon B ^a   Roman, Alejandro J ^a   Windsor, Elizabeth A M ^a   Steinberg, Janet D ^a   Branham, Kart ^b   Othman, Mohammad ^b   Swaroop, Anand ^b   Jacobson, Samuel G ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

^b UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ANALYTIC METHOD; ARTICLE; CHILD; CLINICAL ARTICLE; COMPARATIVE STUDY; CONTROLLED STUDY; GENE; GENE MUTATION; HUMAN; OPTICAL COHERENCE TOMOGRAPHY; PHOTORECEPTOR; PRIORITY JOURNAL; RETINA DISEASE; RETINA FOVEA; RETINAL THICKNESS; RETINITIS PIGMENTOSA; RETINITIS PIGMENTOSA GTPASE REGULATOR GENE; THICKNESS; GENETICS; GLIA; MIDDLE AGED; MUTATION; NERVE CELL; PATHOLOGY; PRESCHOOL CHILD; RETINA; X CHROMOSOME LINKED DISORDER;

EYE PROTEIN; RPGR PROTEIN, HUMAN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; EYE PROTEINS; GENETIC DISEASES, X-LINKED; HUMANS; MIDDLE AGED; MUTATION; NEUROGLIA; NEURONS; RETINA; RETINITIS PIGMENTOSA; TOMOGRAPHY, OPTICAL COHERENCE;

EID: 35748950724     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: 10.1167/iovs.07-0453     Document Type: Article

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