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Analysis of myocilin mutations in 1703 glaucoma patients from five different populations.
Hum Mol Genet. 1999 May;8(5):899-905. doi: 10.1093/hmg/8.5.899.
Hum Mol Genet. 1999.
PMID: 10196380
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.
Haider NB, Jacobson SG, Cideciyan AV, Swiderski R, Streb LM, Searby C, Beck G, Hockey R, Hanna DB, Gorman S, Duhl D, Carmi R, Bennett J, Weleber RG, Fishman GA, Wright AF, Stone EM, Sheffield VC.
Haider NB, et al.
Nat Genet. 2000 Feb;24(2):127-31. doi: 10.1038/72777.
Nat Genet. 2000.
PMID: 10655056
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Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR gene.
Fishman GA, Stone EM, Grover S, Derlacki DJ, Haines HL, Hockey RR.
Fishman GA, et al. Among authors: hockey rr.
Arch Ophthalmol. 1999 Apr;117(4):504-10. doi: 10.1001/archopht.117.4.504.
Arch Ophthalmol. 1999.
PMID: 10206579
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Allelic variation in ABCR associated with Stargardt disease but not age-related macular degeneration.
Stone EM, Webster AR, Vandenburgh K, Streb LM, Hockey RR, Lotery AJ, Sheffield VC.
Stone EM, et al. Among authors: hockey rr.
Nat Genet. 1998 Dec;20(4):328-9. doi: 10.1038/3798.
Nat Genet. 1998.
PMID: 9843201
No abstract available.
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