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Investigative Ophthalmology & Visual Science|November 1, 1988
Identification of proteins in retinas and IPM from eyes with retinitis pigmentosaS Y Schmidt, C A Heth, R B Edwards, et al.
American Journal of Human Genetics|April 3, 2001
Null RPGRIP1 alleles in patients with Leber congenital amaurosisT P Dryja, S M Adams, J L Grimsby, et al.
Investigative Ophthalmology & Visual Science|December 17, 2008
A homozygous missense mutation in the IRBP gene (RBP3) associated with autosomal recessive retinitis pigmentosaAnneke I den Hollander, Terri L McGee, Carmela Ziviello, et al.
Investigative Ophthalmology & Visual Science|August 31, 2001
Clinical features and mutations in patients with dominant retinitis pigmentosa-1 (RP1)E L Berson, J L Grimsby, S M Adams, et al.
Nature|January 25, 1990
A point mutation of the rhodopsin gene in one form of retinitis pigmentosaT P Dryja, T L McGee, E Reichel, et al.
The New England Journal of Medicine|November 8, 1990
Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosaT P Dryja, T L McGee, L B Hahn, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 23, 2005
Night blindness and abnormal cone electroretinogram ON responses in patients with mutations in the GRM6 gene encoding mGluR6Thaddeus P Dryja, Terri L McGee, Eliot L Berson, et al.
Molecular Vision|June 25, 2014
Mutational screening of splicing factor genes in cases with autosomal dominant retinitis pigmentosaPaola Benaglio, Patricia Fernandez San Jose, Almudena Avila-Fernandez, et al.
Human Gene Therapy|April 14, 2010
Replacement gene therapy with a human RPGRIP1 sequence slows photoreceptor degeneration in a murine model of Leber congenital amaurosisBasil S Pawlyk, Oleg V Bulgakov, Xiaoqing Liu, et al.
Molecular Vision|March 28, 2009
Search for a correlation between telomere length and severity of retinitis pigmentosa due to the dominant rhodopsin Pro23His mutationDyonne T Hartong, Terri L McGee, Michael A Sandberg, et al.
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