메뉴 건너뛰기




Volumn 42, Issue 3, 1998, Pages 186-192

Analysis of Peripherin/RDS gene for japanese retinal dystrophies

Author keywords

DNA polymorphism; Macular dystrophy; Peripherin RDS; Retinal dystrophy; Retinitis pigmentosa

Indexed keywords

ASPARTIC ACID; DNA FRAGMENT; GLUTAMIC ACID; GLUTAMINE; GLYCINE; PERIPHERIN;

EID: 0032077856     PISSN: 00215155     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0021-5155(97)00133-0     Document Type: Article
Times cited : (10)

References (44)
  • 1
    • 0026596042 scopus 로고
    • Localization of peripherin/rds in the disk membranes of cone and rod photoreceptors: Relationship to disc membrane morphogenesis and retinal degeneration
    • Arikawa K., Molday L.L., Molday R.S., Williams D.S. Localization of peripherin/rds in the disk membranes of cone and rod photoreceptors. Relationship to disc membrane morphogenesis and retinal degeneration J Cell Biol. 116:1992;659-667.
    • (1992) J Cell Biol , vol.116 , pp. 659-667
    • Arikawa, K.1    Molday, L.L.2    Molday, R.S.3    Williams, D.S.4
  • 2
    • 0026053969 scopus 로고
    • The retinal degeneration slow(rds) gene product is a photoreceptor disc membrane-associated glycoprotein
    • Travis G.H., Sutcliffe J.G., Bok D. The retinal degeneration slow(rds) gene product is a photoreceptor disc membrane-associated glycoprotein. Neuron. 6:1991;61-70.
    • (1991) Neuron , vol.6 , pp. 61-70
    • Travis, G.H.1    Sutcliffe, J.G.2    Bok, D.3
  • 3
    • 0025827541 scopus 로고
    • The human retinal degeneration slow (Rds) gene: Chromosome assignment and structure of the mRNA
    • Travis G.H., Christerson L., Danielson P.E.et al. The human retinal degeneration slow (Rds) gene. Chromosome assignment and structure of the mRNA Genomics. 10:1991;733-739.
    • (1991) Genomics , vol.10 , pp. 733-739
    • Travis, G.H.1    Christerson, L.2    Danielson, P.E.3
  • 4
    • 0025721075 scopus 로고
    • A three-base-pair deletion in the peripherin-Rds gene in one form of retinitis pigmentosa
    • Farrar G.J., Kenna P., Jordan S.A.et al. A three-base-pair deletion in the peripherin-Rds gene in one form of retinitis pigmentosa. Nature. 354:1991;478-480.
    • (1991) Nature , vol.354 , pp. 478-480
    • Farrar, G.J.1    Kenna, P.2    Jordan, S.A.3
  • 5
    • 0025720710 scopus 로고
    • Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa
    • Kajiwara K., Hahn L.B., Mukai S., Travis G.H., Berson E.L., Dryja T.P. Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. Nature. 354:1991;480-483.
    • (1991) Nature , vol.354 , pp. 480-483
    • Kajiwara, K.1    Hahn, L.B.2    Mukai, S.3    Travis, G.H.4    Berson, E.L.5    Dryja, T.P.6
  • 6
    • 0027401094 scopus 로고
    • Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene
    • Nichols B.E., Sheffield V.C., Vandenburgh K., Drack A.V., Kimura A.E., Stone E.M. Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene. Nat Genet. 3:1993;202-207.
    • (1993) Nat Genet , vol.3 , pp. 202-207
    • Nichols, B.E.1    Sheffield, V.C.2    Vandenburgh, K.3    Drack, A.V.4    Kimura, A.E.5    Stone, E.M.6
  • 7
    • 0027528652 scopus 로고
    • A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens
    • Kajiwara K., Sandberg M.A., Berson E.L., Dryja T.P. A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens. Nat Genet. 3:1993;208-212.
    • (1993) Nat Genet , vol.3 , pp. 208-212
    • Kajiwara, K.1    Sandberg, M.A.2    Berson, E.L.3    Dryja, T.P.4
  • 8
    • 0027253598 scopus 로고
    • A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea
    • Nichols B.E., Drack A.V., Vandenburgh K., Kimura A.E., Sheffield V.C., Stone E.M. A 2 base pair deletion in the RDS gene associated with butterfly-shaped pigment dystrophy of the fovea. Hum Mol Genet. 2:1993;601-603.
    • (1993) Hum Mol Genet , vol.2 , pp. 601-603
    • Nichols, B.E.1    Drack, A.V.2    Vandenburgh, K.3    Kimura, A.E.4    Sheffield, V.C.5    Stone, E.M.6
  • 9
    • 0027447531 scopus 로고
    • Mutations in the human retinal degeneration slow (Rds) gene can cause either retinitis pigmentosa or macular dystrophy
    • Wells J., Wroblewski J., Keen J.et al. Mutations in the human retinal degeneration slow (Rds) gene can cause either retinitis pigmentosa or macular dystrophy. Nat Genet. 3:1993;213-218.
    • (1993) Nat Genet , vol.3 , pp. 213-218
    • Wells, J.1    Wroblewski, J.2    Keen, J.3
  • 10
    • 0027434085 scopus 로고
    • Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/Rds gene
    • Weleber R.G., Carr R.E., Murphey W.H., Sheffield V.C., Stone E.M. Phenotypic variation including retinitis pigmentosa, pattern dystrophy, and fundus flavimaculatus in a single family with a deletion of codon 153 or 154 of the peripherin/Rds gene. Arch Ophthalmol. 111:1993;1531-1542.
    • (1993) Arch Ophthalmol , vol.111 , pp. 1531-1542
    • Weleber, R.G.1    Carr, R.E.2    Murphey, W.H.3    Sheffield, V.C.4    Stone, E.M.5
  • 11
    • 0028010027 scopus 로고
    • Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow gene
    • Wroblewski J.J., Wells J.A. III, Eckstein A.et al. Macular dystrophy associated with mutations at codon 172 in the human retinal degeneration slow gene. Ophthalmology. 101:1994;12-22.
    • (1994) Ophthalmology , vol.101 , pp. 12-22
    • Wroblewski, J.J.1    Wells J.A. III2    Eckstein, A.3
  • 12
    • 0028069944 scopus 로고
    • RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function
    • Kemp C.M., Jacobson S.G., Cideciyan A.V., Kimura A.E., Sheffield V.C., Stone E.M. RDS gene mutations causing retinitis pigmentosa or macular degeneration lead to the same abnormality in photoreceptor function. Invest Ophthalmol Vis Sci. 35:1994;3154-3162.
    • (1994) Invest Ophthalmol Vis Sci , vol.35 , pp. 3154-3162
    • Kemp, C.M.1    Jacobson, S.G.2    Cideciyan, A.V.3    Kimura, A.E.4    Sheffield, V.C.5    Stone, E.M.6
  • 13
    • 0028914509 scopus 로고
    • Autosomal dominant pattern dystrophy of the retina associated with a 4-base pair insertion at codon 140 in the peripherin/Rds gene
    • Kim R.Y., Dollfus H., Keen T.J.et al. Autosomal dominant pattern dystrophy of the retina associated with a 4-base pair insertion at codon 140 in the peripherin/Rds gene. Arch Ophthalmol. 113:1995;451-455.
    • (1995) Arch Ophthalmol , vol.113 , pp. 451-455
    • Kim, R.Y.1    Dollfus, H.2    Keen, T.J.3
  • 14
    • 0027373291 scopus 로고
    • A novel Cys-214-Ser mutation in the peripherin/RDS gene in a Japanese family with autosomal dominant retinitis pigmentosa
    • Saga M., Mashima Y., Akeo K., Oguchi Y., Kudoh J., Shimizu N. A novel Cys-214-Ser mutation in the peripherin/RDS gene in a Japanese family with autosomal dominant retinitis pigmentosa. Hum Genet. 92:1993;519-521.
    • (1993) Hum Genet , vol.92 , pp. 519-521
    • Saga, M.1    Mashima, Y.2    Akeo, K.3    Oguchi, Y.4    Kudoh, J.5    Shimizu, N.6
  • 15
    • 0028181667 scopus 로고
    • A novel mutation (Asn244Lys) in the peripherin/RDS gene causing autosomal dominant retinitis pigmentosa associated with bull's-eye maculopathy detected by nonradioisotopic SSCP
    • Kikawa E., Nakazawa M., Chida Y., Shiono T., Tamai M. A novel mutation (Asn244Lys) in the peripherin/RDS gene causing autosomal dominant retinitis pigmentosa associated with bull's-eye maculopathy detected by nonradioisotopic SSCP. Genomics. 20:1994;137-139.
    • (1994) Genomics , vol.20 , pp. 137-139
    • Kikawa, E.1    Nakazawa, M.2    Chida, Y.3    Shiono, T.4    Tamai, M.5
  • 16
    • 0028279531 scopus 로고
    • Asn244His mutation of the peripherin/RDS gene causing autosomal dominant cone-rod degeneration
    • Nakazawa M., Kikawa E., Chida Y., Tamai M. Asn244His mutation of the peripherin/RDS gene causing autosomal dominant cone-rod degeneration. Hum Mol Genet. 3:1994;1195-1196.
    • (1994) Hum Mol Genet , vol.3 , pp. 1195-1196
    • Nakazawa, M.1    Kikawa, E.2    Chida, Y.3    Tamai, M.4
  • 17
    • 0029589288 scopus 로고
    • Macular dystrophy associated with monogenic Arg172Trp mutation of the peripherin/RDS gene in a Japanese family
    • Nakazawa M., Wada Y., Tamai M. Macular dystrophy associated with monogenic Arg172Trp mutation of the peripherin/RDS gene in a Japanese family. Retina. 15:1995;518-523.
    • (1995) Retina , vol.15 , pp. 518-523
    • Nakazawa, M.1    Wada, Y.2    Tamai, M.3
  • 18
    • 0030045140 scopus 로고    scopus 로고
    • Autosomal dominant cone-rod dystrophy associated with mutations in codon 244 (Asn244His) and codon 184 (Tyr184Ser) of the peripherin/Rds gene
    • Nakazawa M., Kikawa E., Chida Y., Wada Y., Shiono T., Tamai M. Autosomal dominant cone-rod dystrophy associated with mutations in codon 244 (Asn244His) and codon 184 (Tyr184Ser) of the peripherin/Rds gene. Arch Ophthalmol. 114:1996;72-78.
    • (1996) Arch Ophthalmol , vol.114 , pp. 72-78
    • Nakazawa, M.1    Kikawa, E.2    Chida, Y.3    Wada, Y.4    Shiono, T.5    Tamai, M.6
  • 19
    • 0028245437 scopus 로고
    • Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/Rds and Rom1 loci
    • Kajiwara K., Berson E.L., Dryja T.P. Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/Rds and Rom1 loci. Science. 264:1994;1604-1608.
    • (1994) Science , vol.264 , pp. 1604-1608
    • Kajiwara, K.1    Berson, E.L.2    Dryja, T.P.3
  • 20
    • 0024756969 scopus 로고
    • Rapid and sensitive detection of point mutations and DNA polymorphism using the polymerase chain reaction
    • Orita M., Suzuki Y., Sekiya T., Hayashi K. Rapid and sensitive detection of point mutations and DNA polymorphism using the polymerase chain reaction. Genomics. 5:1989;874-879.
    • (1989) Genomics , vol.5 , pp. 874-879
    • Orita, M.1    Suzuki, Y.2    Sekiya, T.3    Hayashi, K.4
  • 22
    • 0025371311 scopus 로고
    • Molecular cloning, primary structure, and orientation of the vertebrate photoreceptor cell protein peripherin in the rod outer segment disk membrane
    • Connell G.J., Molday R.S. Molecular cloning, primary structure, and orientation of the vertebrate photoreceptor cell protein peripherin in the rod outer segment disk membrane. Biochemistry. 29:1990;4691-4698.
    • (1990) Biochemistry , vol.29 , pp. 4691-4698
    • Connell, G.J.1    Molday, R.S.2
  • 23
    • 0024571803 scopus 로고
    • Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)
    • Travis G.H., Brennan M.B., Danielson P.E., Kozak C.A., Sutcliffe J.G. Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds). Nature. 338:1989;70-73.
    • (1989) Nature , vol.338 , pp. 70-73
    • Travis, G.H.1    Brennan, M.B.2    Danielson, P.E.3    Kozak, C.A.4    Sutcliffe, J.G.5
  • 24
    • 0025375038 scopus 로고
    • Nucleotide and predicted protein sequence of rat retinal degeneration slow (rds)
    • Begy C., Bridges C.D. Nucleotide and predicted protein sequence of rat retinal degeneration slow (rds). Nucleic Acids Res. 18:1990;3058.
    • (1990) Nucleic Acids Res , vol.18 , pp. 3058
    • Begy, C.1    Bridges, C.D.2
  • 25
    • 0027652897 scopus 로고
    • The cat RDS transcript: Candidate gene analysis and phylogenetic sequence analysis
    • Gorin M.B., Snyder S., To A., Narfstrom K., Curtis R. The cat RDS transcript. Candidate gene analysis and phylogenetic sequence analysis Mamm Genome. 4:1993;544-548.
    • (1993) Mamm Genome , vol.4 , pp. 544-548
    • Gorin, M.B.1    Snyder, S.2    To, A.3    Narfstrom, K.4    Curtis, R.5
  • 26
    • 0010456244 scopus 로고
    • Screen for mutations in the entire coding sequence of the human Rds/peripherin gene in patients with hereditary retinal degenerations
    • Kajiwara K., Berson E.L., Dryja T.P. Screen for mutations in the entire coding sequence of the human Rds/peripherin gene in patients with hereditary retinal degenerations. Invest Ophthalmol Vis Sci. 34:1993;1149.
    • (1993) Invest Ophthalmol Vis Sci , vol.34 , pp. 1149
    • Kajiwara, K.1    Berson, E.L.2    Dryja, T.P.3
  • 27
    • 0026669047 scopus 로고
    • Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (Adrp)
    • Fujiki K., Hotta Y., Hayakawa M.et al. Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (Adrp). Jpn J Hum Genet. 37:1992;125-132.
    • (1992) Jpn J Hum Genet , vol.37 , pp. 125-132
    • Fujiki, K.1    Hotta, Y.2    Hayakawa, M.3
  • 28
    • 0028861972 scopus 로고
    • Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa
    • Fujiki K., Hotta Y., Murakami A.et al. Missense mutation of rhodopsin gene codon 15 found in Japanese autosomal dominant retinitis pigmentosa. Jpn J Hum Genet. 40:1995;271-277.
    • (1995) Jpn J Hum Genet , vol.40 , pp. 271-277
    • Fujiki, K.1    Hotta, Y.2    Murakami, A.3
  • 29
    • 0027516347 scopus 로고
    • Clinical features of autosomal dominant retinitis pigmentosa with rhodopsin gene codon 17 mutation and retinal neovascularization in a Japanese patient
    • Hayakawa M., Hotta Y., Imai Y.et al. Clinical features of autosomal dominant retinitis pigmentosa with rhodopsin gene codon 17 mutation and retinal neovascularization in a Japanese patient. Am J Ophthalmol. 115:1993;168-173.
    • (1993) Am J Ophthalmol , vol.115 , pp. 168-173
    • Hayakawa, M.1    Hotta, Y.2    Imai, Y.3
  • 30
    • 0028088437 scopus 로고
    • Autosomal dominant retinitis pigmentosa: A mutation in codon 181 (Glu→Lys) of the rhodopsin gene in a Japanese family
    • Saga M., Mashima Y., Akeo K., Oguchi Y., Kudoh J., Shimizu N. Autosomal dominant retinitis pigmentosa. A mutation in codon 181 (Glu→Lys) of the rhodopsin gene in a Japanese family Ophthalmic Genet. 15:1994;61-67.
    • (1994) Ophthalmic Genet , vol.15 , pp. 61-67
    • Saga, M.1    Mashima, Y.2    Akeo, K.3    Oguchi, Y.4    Kudoh, J.5    Shimizu, N.6
  • 31
    • 0027155177 scopus 로고
    • Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q
    • Jordan S.A., Farrar G.J., Kenna P.et al. Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7q. Nat Genet. 4:1993;54-58.
    • (1993) Nat Genet , vol.4 , pp. 54-58
    • Jordan, S.A.1    Farrar, G.J.2    Kenna, P.3
  • 32
    • 0028831395 scopus 로고
    • Evidence for a major gene (Rp10) for autosomal dominant retinitis pigmentosa on chromosome 7q: Linkage mapping in a second, unrelated family
    • McGuire R.E., Gannon A.M., Sullivan L.S., Rodriguez J.A., Daiger S.P. Evidence for a major gene (Rp10) for autosomal dominant retinitis pigmentosa on chromosome 7q. Linkage mapping in a second, unrelated family Hum Genet. 95:1995;71-74.
    • (1995) Hum Genet , vol.95 , pp. 71-74
    • McGuire, R.E.1    Gannon, A.M.2    Sullivan, L.S.3    Rodriguez, J.A.4    Daiger, S.P.5
  • 33
    • 0027309259 scopus 로고
    • A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p
    • Inglehearn C.F., Carter S.A., Keen T.J.et al. A new locus for autosomal dominant retinitis pigmentosa on chromosome 7p. Nat Genet. 4:1993;51-53.
    • (1993) Nat Genet , vol.4 , pp. 51-53
    • Inglehearn, C.F.1    Carter, S.A.2    Keen, T.J.3
  • 34
    • 0026347736 scopus 로고
    • Linkage mapping of autosomal dominant retinitis pigmentosa (Rp1) to the pericentric region of human chromosome 8
    • Blanton S.H., Heckenlively J.R., Cottingham A.W.et al. Linkage mapping of autosomal dominant retinitis pigmentosa (Rp1) to the pericentric region of human chromosome 8. Genomics. 11:1991;857-869.
    • (1991) Genomics , vol.11 , pp. 857-869
    • Blanton, S.H.1    Heckenlively, J.R.2    Cottingham, A.W.3
  • 35
    • 0028363788 scopus 로고
    • A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17
    • Greenberg J., Goliath R., Beighton P., Ramesar R. A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17. Hum Mol Genet. 3:1994;915-918.
    • (1994) Hum Mol Genet , vol.3 , pp. 915-918
    • Greenberg, J.1    Goliath, R.2    Beighton, P.3    Ramesar, R.4
  • 36
    • 0028123295 scopus 로고
    • Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19
    • Al-Maghtheh M., Inglehearn C.F., Keen T.J.et al. Identification of a sixth locus for autosomal dominant retinitis pigmentosa on chromosome 19. Hum Mol Genet. 3:1994;351-354.
    • (1994) Hum Mol Genet , vol.3 , pp. 351-354
    • Al-Maghtheh, M.1    Inglehearn, C.F.2    Keen, T.J.3
  • 37
    • 0027933727 scopus 로고
    • Assignment of a gene for autosomal recessive retinitis pigmentosa (Rp12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population
    • van Soest S., van den Born L.I., Gal A.et al. Assignment of a gene for autosomal recessive retinitis pigmentosa (Rp12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population. Genomics. 22:1994;499-504.
    • (1994) Genomics , vol.22 , pp. 499-504
    • Van Soest, S.1    Van Den Born, L.I.2    Gal, A.3
  • 38
    • 0027270053 scopus 로고
    • Recessive mutations in the gene encoding the β-subunit of phosphodiesterase in patients with retinitis pigmentosa
    • McLaughlin M.E., Sandberg M.A., Berson E.L., Dryja T.P. Recessive mutations in the gene encoding the β-subunit of phosphodiesterase in patients with retinitis pigmentosa. Nat Genet. 4:1993;130-134.
    • (1993) Nat Genet , vol.4 , pp. 130-134
    • McLaughlin, M.E.1    Sandberg, M.A.2    Berson, E.L.3    Dryja, T.P.4
  • 39
    • 0028789921 scopus 로고
    • Autosomal recessive retinitis pigmentosa caused by mutations in the α subunit of rod cGMP phosphodiesterase
    • Huang S.H., Pittler S., Huang X., Oliveira L., Berson E.L., Dryja T.P. Autosomal recessive retinitis pigmentosa caused by mutations in the α subunit of rod cGMP phosphodiesterase. Nat Genet. 11:1995;468-471.
    • (1995) Nat Genet , vol.11 , pp. 468-471
    • Huang, S.H.1    Pittler, S.2    Huang, X.3    Oliveira, L.4    Berson, E.L.5    Dryja, T.P.6
  • 40
    • 0028820045 scopus 로고
    • Mutations in the gene encoding the α subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa
    • Dryja T.P., Finn J.T., Peng Y.-W., McGee T.L., Berson E.L., Yau K.-W. Mutations in the gene encoding the α subunit of the rod cGMP-gated channel in autosomal recessive retinitis pigmentosa. Proc Natl Acad Sci USA. 92:1995;10177-10181.
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 10177-10181
    • Dryja, T.P.1    Finn, J.T.2    Peng, Y.-W.3    McGee, T.L.4    Berson, E.L.5    Yau, K.-W.6
  • 41
    • 0026895234 scopus 로고
    • Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13
    • Stone E.M., Nichols B.E., Streb L.M., Kimura A.E., Sheffield V.C. Genetic linkage of vitelliform macular degeneration (Best's disease) to chromosome 11q13. Nat Genet. 1:1992;246-250.
    • (1992) Nat Genet , vol.1 , pp. 246-250
    • Stone, E.M.1    Nichols, B.E.2    Streb, L.M.3    Kimura, A.E.4    Sheffield, V.C.5
  • 42
    • 0027030392 scopus 로고
    • Polymorphic variation within "Conserved" sequences at the 3′ end of the human RDS gene which results in amino acid substitutions
    • Jordan S.A., Farrar G.J., Kenna P., Humphries P. Polymorphic variation within "Conserved" sequences at the 3′ end of the human RDS gene which results in amino acid substitutions. Hum Mutat. 1:1992;240-247.
    • (1992) Hum Mutat , vol.1 , pp. 240-247
    • Jordan, S.A.1    Farrar, G.J.2    Kenna, P.3    Humphries, P.4
  • 43
    • 0029015292 scopus 로고
    • Frequencies of polymorphisms in the rhodopsin gene of Japanese retinitis pigmentosa and normal individuals
    • Fujiki K., Kawano H., Hotta Y.et al. Frequencies of polymorphisms in the rhodopsin gene of Japanese retinitis pigmentosa and normal individuals. Jpn J Hum Genet. 40:1995;203-206.
    • (1995) Jpn J Hum Genet , vol.40 , pp. 203-206
    • Fujiki, K.1    Kawano, H.2    Hotta, Y.3
  • 44
    • 0026209385 scopus 로고
    • Rhodopsin mutations in autosomal dominant retinitis pigmentosa
    • Sung C.H., Davenport C.M., Hennessey J.C.et al. Rhodopsin mutations in autosomal dominant retinitis pigmentosa. Proc Natl Acad Sci USA. 88:1991;6481-6485.
    • (1991) Proc Natl Acad Sci USA , vol.88 , pp. 6481-6485
    • Sung, C.H.1    Davenport, C.M.2    Hennessey, J.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.