Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa
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E. Zrenner | A. Gal | F. Prieto | J. M. Millán | M. Beneyto | Rosabel Bosch | Moritz Meins | Eckart Apfelstedt‐Sylla | Gunnar Grüning | Manuel Caballero
[1] V. Sheffield,et al. A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea. , 1993, Human molecular genetics.
[2] J. Ott,et al. Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosa. , 1993, Genomics.
[3] Alan Bird,et al. Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy , 1993, Nature Genetics.
[4] V. Sheffield,et al. Butterfly–shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene , 1993, Nature Genetics.
[5] J. E. Hepler,et al. A medley of retinal dystrophies , 1993, Nature Genetics.
[6] P. Humphries,et al. A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa , 1991, Nature.
[7] T. Dryja,et al. Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa , 1991, Nature.
[8] J. Sutcliffe,et al. The human retinal degeneration slow (RDS) gene: chromosome assignment and structure of the mRNA. , 1991, Genomics.