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Volumn 61, Issue 6, 1997, Pages 1448-1450

Homogeneity of kerato-epithelin codon 124 mutations in Japanese patients with either of two types of corneal stromal dystrophy [2]

Author keywords

[No Author keywords available]

Indexed keywords

AMYLOID; DNA;

EID: 0031454598     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301649     Document Type: Letter
Times cited : (47)

References (19)
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  • 2
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    • MD Brown A Torroni CL Reckord DC Wallace Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations Hum Mutat 6 1995 311 325
    • (1995) Hum Mutat , vol.6 , pp. 311-325
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  • 3
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    • Clinically atypical granular corneal dystrophy with pathological features of lattice-like amyloid deposits: a study of three families
    • R Folberg E Alfonso O Croxatto NG Driezen N Panjwani PR Laibson SA Boruchoff Clinically atypical granular corneal dystrophy with pathological features of lattice-like amyloid deposits: a study of three families Ophthalmology 95 1988 46 51
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    • Folberg, R1    Alfonso, E2    Croxatto, O3    Driezen, NG4    Panjwani, N5    Laibson, PR6    Boruchoff, SA7
  • 4
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    • The relationship between granular, lattice type 1, and Avellino corneal dystrophies: a histopathologic study
    • R Folberg EM Stone VC Sheffield WD Mathers The relationship between granular, lattice type 1, and Avellino corneal dystrophies: a histopathologic study Arch Ophthalmol 112 1994 1080 1085
    • (1994) Arch Ophthalmol , vol.112 , pp. 1080-1085
    • Folberg, R1    Stone, EM2    Sheffield, VC3    Mathers, WD4
  • 5
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    • A homozygous 1–base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese
    • A Fuchs M Nakazawa M Maw M Tamai Y Oguchi A Gal A homozygous 1–base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese Nat Genet 10 1995 360 362
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  • 6
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    • Histochemistry of corneal granular dystrophy
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    • (1969) Br J Ophthalmol , vol.53 , pp. 799-807
    • Garner, A1
  • 7
    • 0028954349 scopus 로고
    • Genetic refinement of the chromosome 5q lattice corneal dystrophy type I locus to within a 2 cM interval
    • CY Gregory K Evans SS Bhattacharya Genetic refinement of the chromosome 5q lattice corneal dystrophy type I locus to within a 2 cM interval J Med Genet 32 1995 224 226
    • (1995) J Med Genet , vol.32 , pp. 224-226
    • Gregory, CY1    Evans, K2    Bhattacharya, SS3
  • 8
    • 0017365859 scopus 로고
    • Unusual superficial variant of granular dystrophy of the cornea
    • R Haddad RL Font BS Fine Unusual superficial variant of granular dystrophy of the cornea Am J Ophthalmol 83 1977 213 218
    • (1977) Am J Ophthalmol , vol.83 , pp. 213-218
    • Haddad, R1    Font, RL2    Fine, BS3
  • 10
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    • Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees
    • N Howell I Kubacka S Halvorson B Howell DA MaCullough D Mackey Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees Genetics 140 1995 285 302
    • (1995) Genetics , vol.140 , pp. 285-302
    • Howell, N1    Kubacka, I2    Halvorson, S3    Howell, B4    MaCullough, DA5    Mackey, D6
  • 11
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    • Granular-lattice (Avellino) corneal dystrophy in Japanese patients
    • M Konishi Y Mashima Y Nakamura M Yamada H Sugiura Granular-lattice (Avellino) corneal dystrophy in Japanese patients Cornea 16 1997 635 638
    • (1997) Cornea , vol.16 , pp. 635-638
    • Konishi, M1    Mashima, Y2    Nakamura, Y3    Yamada, M4    Sugiura, H5
  • 12
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    • Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOX
    • E Korvatska FL Munier L Zografos F Ahmad R Faggioni A Dolivo-Beuret S Uffer Delineation of a 1-cM region on distal 5q containing the locus for corneal dystrophies Groenouw type I and lattice type I and exclusion of the candidate genes SPARC and LOX Eur J Hum Genet 4 1996 214 218
    • (1996) Eur J Hum Genet , vol.4 , pp. 214-218
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    • Mannis, MJ1    De Sousa, LB2    Gross, RH3
  • 15
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    • SL Owend J Sugar DP Edward Superficial granular corneal dystrophy with amyloid deposits Arch Ophthalmol 110 1992 175 176
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.