메뉴 건너뛰기




Volumn 62, Issue 1, 1998, Pages 122-129

Linkage analysis of X-linked cone-rod dystrophy: Localization to Xp11.4 and definition of a locus distinct from RP2 and RP3

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

EID: 17344363253     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/301667     Document Type: Article
Times cited : (20)

References (21)
  • 1
    • 0000914411 scopus 로고
    • Cone dystrophy (X-linked) (COD1) maps between DXS7 (L1.28) and DXS206 (Xj1.1) and is linked to DXS84
    • Hartley J, Gies C, Jacobson D (1989) Cone dystrophy (X-linked) (COD1) maps between DXS7 (L1.28) and DXS206 (Xj1.1) and is linked to DXS84. Cytogenet Cell Genet 51: 959
    • (1989) Cytogenet Cell Genet , vol.51 , pp. 959
    • Hartley, J.1    Gies, C.2    Jacobson, D.3
  • 2
    • 0027138447 scopus 로고
    • Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3
    • Bergen AAB, Meire F, ten Brink J, Schuurman EJM, van Ommen GB, Delleman JW (1993) Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3. Genomics 18:463-464
    • (1993) Genomics , vol.18 , pp. 463-464
    • Bergen, A.A.B.1    Meire, F.2    Ten Brink, J.3    Schuurman, E.J.M.4    Van Ommen, G.B.5    Delleman, J.W.6
  • 6
    • 0028804575 scopus 로고
    • A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration
    • Gorin MB, Jackson KE, Ferrell RE, Sheffield VC, Jacobson SG, Gass JD, Mitchell E, et al (1995) A peripherin/retinal degeneration slow mutation (Pro-210-Arg) associated with macular and peripheral retinal degeneration. Ophthalmology 102:246-255
    • (1995) Ophthalmology , vol.102 , pp. 246-255
    • Gorin, M.B.1    Jackson, K.E.2    Ferrell, R.E.3    Sheffield, V.C.4    Jacobson, S.G.5    Gass, J.D.6    Mitchell, E.7
  • 7
    • 0028126874 scopus 로고
    • Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1)
    • Hong H-K, Ferrell RE, Gorin MB (1994) Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1). Am J Hum Genet 55:1173-1181
    • (1994) Am J Hum Genet , vol.55 , pp. 1173-1181
    • Hong, H.-K.1    Ferrell, R.E.2    Gorin, M.B.3
  • 8
    • 0024358385 scopus 로고
    • X-linked progressive cone dystrophy: Clinical characteristics of affected males and female carriers
    • Jacobson DM, Thompson HS, Bartley JA (1989) X-linked progressive cone dystrophy: clinical characteristics of affected males and female carriers. Ophthalmology 96:885-895
    • (1989) Ophthalmology , vol.96 , pp. 885-895
    • Jacobson, D.M.1    Thompson, H.S.2    Bartley, J.A.3
  • 10
    • 0029020995 scopus 로고
    • X-linked dominant cone-rod degeneration: Linkage mapping of a new locus for retinitis pigmentosa (RP15) to Xp22.13-p22.11
    • McGuire RE, Sullivan LS, Blanton SH, Church MW, Heckenlively JR, Daiger SP (1995) X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP15) to Xp22.13-p22.11. Am J Hum Genet 57:87-94
    • (1995) Am J Hum Genet , vol.57 , pp. 87-94
    • McGuire, R.E.1    Sullivan, L.S.2    Blanton, S.H.3    Church, M.W.4    Heckenlively, J.R.5    Daiger, S.P.6
  • 11
    • 15844378213 scopus 로고    scopus 로고
    • A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)
    • Meindl A, Dry K, Herrmann K, Manson F, Ciccodicola A, Edgar A, Carvalho MRS, et al (1996) A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3). Nat Genet 13:35-42
    • (1996) Nat Genet , vol.13 , pp. 35-42
    • Meindl, A.1    Dry, K.2    Herrmann, K.3    Manson, F.4    Ciccodicola, A.5    Edgar, A.6    Carvalho, M.R.S.7
  • 12
    • 0027979863 scopus 로고
    • X linked progressive cone dystrophy: Localisation of the gene locus to Xp21-p11.1 by linkage analysis
    • Meire FM, Bergen AAB, De Rouck A, Leys M, Delleman JW (1994) X linked progressive cone dystrophy: localisation of the gene locus to Xp21-p11.1 by linkage analysis. Br J Ophthalmol 78:103-108
    • (1994) Br J Ophthalmol , vol.78 , pp. 103-108
    • Meire, F.M.1    Bergen, A.A.B.2    De Rouck, A.3    Leys, M.4    Delleman, J.W.5
  • 15
    • 0028790963 scopus 로고
    • The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
    • O'Connell JR, Weeks DE (1995) The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet 11:402-408
    • (1995) Nat Genet , vol.11 , pp. 402-408
    • O'Connell, J.R.1    Weeks, D.E.2
  • 19
    • 0028060401 scopus 로고
    • Retinitis pigmentosa and related disorders: Phenotypes of rhodopsin and peripherin/RDS mutations
    • Shastry BS (1994) Retinitis pigmentosa and related disorders: phenotypes of rhodopsin and peripherin/RDS mutations. Am J Med Genet 52:467-474
    • (1994) Am J Med Genet , vol.52 , pp. 467-474
    • Shastry, B.S.1
  • 21
    • 0029841724 scopus 로고    scopus 로고
    • Mapping the RP2 locus for X-linked retinitis pigmentosa on proximal Xp: A genetically defined 5-cM critical region and exclusion of candidate genes by physical mapping
    • Thiselton DL, Hampson RM, Nayudu M, Maldergem LV, Wolf ML, Saha BK, Bhattacharya SS, et al (1996) Mapping the RP2 locus for X-linked retinitis pigmentosa on proximal Xp: a genetically defined 5-cM critical region and exclusion of candidate genes by physical mapping. Genome Res 6: 1093-1102
    • (1996) Genome Res , vol.6 , pp. 1093-1102
    • Thiselton, D.L.1    Hampson, R.M.2    Nayudu, M.3    Maldergem, L.V.4    Wolf, M.L.5    Saha, B.K.6    Bhattacharya, S.S.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.