Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatus
Boon et al.
Br J Ophthalmol 2007;91:1504-1511.
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Molecular Testing for Hereditary Retinal Disease as Part of Clinical Care
Downs et al.
Arch Ophthalmol 2007;125:252-258.
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Intrafamilial phenotypic variability in families with RDS mutations: exclusion of ROM1 as a genetic modifier for those with retinitis pigmentosa
Leroy et al.
Br J Ophthalmol 2007;91:89-93.
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Clinical Findings in a Multigeneration Family With Autosomal Dominant Central Areolar Choroidal Dystrophy Associated With an Arg195Leu Mutation in the Peripherin/RDS Gene
Keilhauer et al.
Arch Ophthalmol 2006;124:1020-1027.
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Spectrum and Frequency of Mutations in IMPDH1 Associated with Autosomal Dominant Retinitis Pigmentosa and Leber Congenital Amaurosis
Bowne et al.
IOVS 2006;47:34-42.
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A Novel Locus for Autosomal Dominant Cone and Cone-Rod Dystrophies Maps to the 6p Gene Cluster of Retinal Dystrophies
Castori et al.
IOVS 2005;46:3539-3544.
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Sequencing Arrays for Screening Multiple Genes Associated with Early-Onset Human Retinal Degenerations on a High-Throughput Platform
Mandal et al.
IOVS 2005;46:3355-3362.
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Genetic and phenotypic heterogeneity in pattern dystrophy
Francis et al.
Br J Ophthalmol 2005;89:1115-1119.
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A novel mutation in the RDS gene in an Italian family with pattern dystrophy
Testa et al.
Br J Ophthalmol 2005;89:1066-1068.
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Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence
Cideciyan et al.
Hum Mol Genet 2004;13:525-534.
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A Peculiar Autosomal Dominant Macular Dystrophy Caused by an Asparagine Deletion at Codon 169 in the Peripherin/RDS Gene
van Lith-Verhoeven et al.
Arch Ophthalmol 2003;121:1452-1457.
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The genetics of inherited macular dystrophies
Michaelides et al.
J. Med. Genet. 2003;40:641-650.
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Late-Onset Autosomal Dominant Macular Dystrophy with Choroidal Neovascularization and Nonexudative Maculopathy Associated with Mutation in the RDS Gene
Khani et al.
IOVS 2003;44:3570-3577.
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The Role of Subunit Assembly in Peripherin-2 Targeting to Rod Photoreceptor Disk Membranes and Retinitis Pigmentosa
Loewen et al.
Mol. Biol. Cell 2003;14:3400-3413.
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Genetic modifiers of vision and hearing
Haider et al.
Hum Mol Genet 2002;11:1195-1206.
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Butterfly-Shaped Pattern Dystrophy: A Genetic, Clinical, and Histopathological Report
Zhang et al.
Arch Ophthalmol 2002;120:485-490.
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Mutations in the RPGR gene cause X-linked cone dystrophy
Yang et al.
Hum Mol Genet 2002;11:605-611.
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Central areolar choroidal dystrophy associated with dominantly inherited drusen
Klevering et al.
Br J Ophthalmol 2002;86:91-96.
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Molecular genetics of age-related macular degeneration
Stone et al.
Hum Mol Genet 2001;10:2285-2292.
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Evaluation of the ELOVL4 gene in families with retinitis pigmentosa linked to the RP25 locus
Li et al.
J. Med. Genet. 2001;38:478-480.
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Ocular Phenotype of Bothnia Dystrophy, an Autosomal Recessive Retinitis Pigmentosa Associated With an R234W Mutation in the RLBP1 Gene
Burstedt et al.
Arch Ophthalmol 2001;119:260-267.
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Autosomal Dominant Cone and Cone-Rod Dystrophy With Mutations in the Guanylate Cyclase Activator 1A Gene-Encoding Guanylate Cyclase Activating Protein-1
Downes et al.
Arch Ophthalmol 2001;119:96-105.
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Mutations in the 11-cis Retinol Dehydrogenase Gene in Japanese Patients with Fundus Albipunctatus
Hirose et al.
IOVS 2000;41:3933-3935.
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Disulfide-mediated Oligomerization of Peripherin/Rds and Rom-1 in Photoreceptor Disk Membranes. IMPLICATIONS FOR PHOTORECEPTOR OUTER SEGMENT MORPHOGENESIS AND DEGENERATION
Loewen and Molday
J. Biol. Chem. 2000;275:5370-5378.
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Autosomal Dominant Macular Atrophy at 6q14 Excludes CORD7 and MCDR1/PBCRA Loci
Griesinger et al.
IOVS 2000;41:248-255.
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Autosomal Dominant Hemorrhagic Macular Dystrophy Not Associated With the TIMP3 Gene
Ayyagari et al.
Arch Ophthalmol 2000;118:85-92.
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Clinical Features of Codon 172 RDS Macular Dystrophy: Similar Phenotype in 12 Families
Downes et al.
Arch Ophthalmol 1999;117:1373-1383.
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Phenotypic variations in a family with retinal dystrophy as result of different mutations in the ABCR gene
Klevering et al.
Br J Ophthalmol 1999;83:914-918.
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Intrafamilial variation of the phenotype in Bardet-Biedl syndrome
Riise et al.
Br J Ophthalmol 1997;81:378-385.
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Defective subunit assembly underlies a digenic form of retinitis pigmentosa linked to mutations in peripherin/rds and rom-1
Goldberg and Molday
Proc. Natl. Acad. Sci. USA 1996;93:13726-13730.
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Deletion in the Peripherin/RDS Gene in Two Unrelated Sardinian Families With Autosomal Dominant Butterfly-Shaped Macular Dystrophy
Fossarello et al.
Arch Ophthalmol 1996;114:448-456.
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Molecular Biology in Ophthalmology: A Review of Principles and Recent Advances
Della
Arch Ophthalmol 1996;114:457-463.
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Three homologs of rds/peripherin in Xenopus laevis photoreceptors that exhibit covalent and non-covalent interactions
Kedzierski et al.
J. Cell Sci. 1996;109:2551-2560.
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Autosomal Dominant Cone-Rod Dystrophy Associated With Mutations in Codon 244 (Asn244His) and Codon 184 (Tyr184Ser) of the Peripherin/RDS Gene
Nakazawa et al.
Arch Ophthalmol 1996;114:72-78.
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Autosomal Dominant Pattern Dystrophy of the Retina Associated With a 4-Base Pair Insertion at Codon 140 in the Peripherin/RDS Gene
Kim et al.
Arch Ophthalmol 1995;113:451-455.
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Autosomal Dominant Macular Dystrophy Simulating North Carolina Macular Dystrophy
Holz et al.
Arch Ophthalmol 1995;113:178-184.
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Ocular Findings in Patients With Autosomal Dominant Retinitis Pigmentosa and Transversion Mutation in Codon 244 (Asn244Lys) of the Peripherin/RDS Gene
Nakazawa et al.
Arch Ophthalmol 1994;112:1567-1573.
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The Relationship Between Granular, Lattice Type 1, and Avellino Corneal Dystrophies: A Histopathologic Study
Folberg et al.
Arch Ophthalmol 1994;112:1080-1085.
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Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci
Kajiwara et al.
Science 1994;264:1604-1608.
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Stargardt's Macular Dystrophy
Weleber
Arch Ophthalmol 1994;112:752-754.
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Clinical Features of a Stargardt-Like Dominant Progressive Macular Dystrophy With Genetic Linkage to Chromosome 6q
Stone et al.
Arch Ophthalmol 1994;112:765-772.
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Molecular Characterization of Peripherin-2 and Rom-1 Mutants Responsible for Digenic Retinitis Pigmentosa
Loewen et al.
J. Biol. Chem. 2001;276:22388-22396.
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