Retinitis pigmentosa and allied diseases: numerous diseases, genes, and inheritance patterns
Rivolta et al.
Hum Mol Genet 2002;11:1219-1227.
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Ocular Findings Associated With Rhodopsin Gene Codon 267 and Codon 190 Mutations in Dominant Retinitis Pigmentosa
Fishman et al.
Arch Ophthalmol 1992;110:1582-1588.
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Ocular Findings Associated With a Rhodopsin Gene Codon 106 Mutation: Glycine-to-Arginine Change in Autosomal Dominant Retinitis Pigmentosa
Fishman et al.
Arch Ophthalmol 1992;110:646-653.
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Ocular Findings Associated With a Rhodopsin Gene Codon 58 Transversion Mutation in Autosomal Dominant Retinitis Pigmentosa
Fishman et al.
Arch Ophthalmol 1991;109:1387-1393.
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Autosomal Dominant Sectoral Retinitis Pigmentosa: Two Families With Transversion Mutation in Codon 23 of Rhodopsin
Heckenlively et al.
Arch Ophthalmol 1991;109:84-91.
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Ocular Findings in Patients With Autosomal Dominant Retinitis Pigmentosa and a Rhodopsin Gene Defect (Pro-23-His)
Berson et al.
Arch Ophthalmol 1991;109:92-101.
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Electroretinography and Retinitis Pigmentosa: No Discrimination Between Genetic Subtypes
Rothberg et al.
Arch Ophthalmol 1982;100:1422-1426.
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Vision Threshold Profiles in Sector Retinitis Pigmentosa
Massof and Finkelstein
Arch Ophthalmol 1979;97:1899-1904.
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A Full-Field System for Clinical Electroretinography
Rabin and Berson
Arch Ophthalmol 1974;92:59-63.
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