Identification of the gene responsible for Best macular dystrophy
K. Petrukhin;M. J. Koisti;B. Bakall;Wen Li.
Nature Genetics (1998)
Mutations in ABCC6 cause pseudoxanthoma elasticum.
A.A. Bergen;A.S. Plomp;E.J. Schuurman;S. Terry.
Nature Genetics (2000)
Autosomal Recessive Retinitis Pigmentosa and Cone-rod Dystrophy Caused by Splice Site Mutations in the Stargardt's Disease Gene ABCR
F.P.M. Cremers;T.J.R. van de Pol;M.A. van Driel;A.I. den Hollander.
Human Molecular Genetics (1998)
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).
A.I. den Hollander;J.B. ten Brink;Y.J.M. de Kok;S. van Soest.
Nature Genetics (1999)
The dynamic nature of Bruch's membrane
J.C. Booij;D.C. Baas;J. Beisekeeva;T.G.M.F. Gorgels.
Progress in Retinal and Eye Research (2010)
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Virginie J M Verhoeven;Pirro G Hysi;Robert Wojciechowski;Robert Wojciechowski;Qiao Fan.
Nature Genetics (2013)
Positional cloning of the gene for X-linked retinitis pigmentosa 2
U. Schwahn;S. Lenzner;J Dong;S. Feil.
Nature Genetics (1998)
Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration.
Dominiek D. G. Despriet;Caroline C. W. Klaver;Jacqueline C. M. Witteman;Arthur A. B. Bergen.
JAMA (2006)
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
N.Torben Bech-Hansen;Margaret J. Naylor;Tracy A. Maybaum;Rebecca L. Sparkes.
Nature Genetics (2000)
Retinitis pigmentosa: defined from a molecular point of view.
S. van Soest;A. Westerveld;P.T.V.M. de Jong;E.M. Bleeker-Wagemakers.
Survey of Ophthalmology (1999)
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