Published in Exp Eye Res on April 27, 2006
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ADAMTSL4, a secreted glycoprotein widely distributed in the eye, binds fibrillin-1 microfibrils and accelerates microfibril biogenesis. Invest Ophthalmol Vis Sci (2012) 0.97
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Thirty-year follow-up of a patient with leber congenital amaurosis and novel RPE65 mutations. Am J Ophthalmol (2004) 0.90
Introducing a new computer-based test for the clinical evaluation of color discrimination. Am J Ophthalmol (2006) 0.90
A novel mutation in the RDS/Peripherin gene causes adult-onset foveomacular dystrophy. Am J Ophthalmol (2003) 0.90
Choroideremia: effect of age on visual acuity in patients and female carriers. Ophthalmic Genet (2011) 0.90
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Slipped, severed, torn and lost extraocular muscles. Can J Ophthalmol (2011) 0.89
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Mutations in KIF21A are responsible for CFEOM1 worldwide. Ophthalmic Genet (2004) 0.86
Retinal Dystrophy with Intraretinal Cystoid Spaces Associated with Mutations in the Crumbs Homologue (CRB1) Gene. Ophthalmic Genet (2015) 0.86
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Nonselective assembly of fibrillin 1 and fibrillin 2 in the rodent ocular zonule and in cultured cells: implications for Marfan syndrome. Invest Ophthalmol Vis Sci (2013) 0.85
CNGA3 mutations in two United Arab Emirates families with achromatopsia. Mol Vis (2008) 0.85
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment development. Am J Hum Genet (2012) 0.85
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Incidence of choroidal neovascularization in the fellow eye in the comparison of age-related macular degeneration treatments trials. Ophthalmology (2013) 0.84
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Lumpers or splitters? The role of molecular diagnosis in Leber congenital amaurosis. Ophthalmic Genet (2006) 0.84
Immunocytochemical evidence of Tulp1-dependent outer segment protein transport pathways in photoreceptor cells. Exp Eye Res (2011) 0.84
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Protective effect of paraoxonase 1 gene variant Gln192Arg in age-related macular degeneration. Am J Ophthalmol (2009) 0.82