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Disease Course in Patients with Autosomal Recessive Retinitis Pigmentosa due to theUSH2AGene
Author(s) -
Michael A. Sandberg,
Bernard Rosner,
Carol Weigel-DiFranco,
Terri L. McGee,
Thaddeus P. Dryja,
Eliot L. Berson
Publication year - 2008
Publication title -
investigative ophthalmology and visual science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.935
H-Index - 218
eISSN - 1552-5783
pISSN - 0146-0404
DOI - 10.1167/iovs.08-2009
Subject(s) - retinitis pigmentosa , visual acuity , ophthalmology , mutation , electroretinography , biology , usher syndrome , medicine , retinal , genetics , gene
To estimate the mean rates of ocular function loss in patients with autosomal recessive retinitis pigmentosa due to USH2A mutations.

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