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Clinical and Experimental Ophthalmology
Volumn 42, Issue 1, 2014, Pages 94-96
Mapping the disease gene in two congenital motor nystagmus families
Author keywords

[No Author keywords available]
Indexed keywords

AUTOSOMAL DOMINANT INHERITANCE; CLINICAL ARTICLE; CONGENITAL NYSTAGMUS; DOMINANT INHERITANCE; FAMILIAL DISEASE; GENE FREQUENCY; GENE LOCUS; GENE MUTATION; GENE SILENCING; GENETIC DISTANCE; GENETIC LINKAGE; HAPLOTYPE; HUMAN; INHERITANCE; LETTER; LINKAGE ANALYSIS; MICROSATELLITE MARKER; X CHROMOSOME;
EID: 84892531760     PISSN: 14426404     EISSN: 14429071     Source Type: Journal    
DOI: 10.1111/ceo.12202     Document Type: Letter
Times cited : (1)
References (8)
  • 1
    • 13544259670 scopus 로고    scopus 로고
    • The effects of increased visual task demand on foveation in congenital nystagmus
    • Tkalcevic LA, Abel LA. The effects of increased visual task demand on foveation in congenital nystagmus. Vision Res 2002; 45: 1139-1146.
    • (2002) Vision Res , vol.45 , pp. 1139-1146
    • Tkalcevic, L.A.1    Abel, L.A.2
  • 2
    • 31544452824 scopus 로고    scopus 로고
    • Linkage analysis of two families with X-linked recessive congenital motor nystagmus
    • Guo XM, Li SQ, Jiang XY, Xiao XS, Wang PF, Zhang QJ. Linkage analysis of two families with X-linked recessive congenital motor nystagmus. J Hum Genet 2006; 51: 76-80.
    • (2006) J Hum Genet , vol.51 , pp. 76-80
    • Guo, X.M.1    Li, S.Q.2    Jiang, X.Y.3    Xiao, X.S.4    Wang, P.F.5    Zhang, Q.J.6
  • 4
    • 0033406864 scopus 로고    scopus 로고
    • Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient
    • Mellott ML, Brown JJ, Fingert JH, Taylor CM, Keech RV, Sheffield VC. Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient. Arch Ophthalmol 1999; 117: 1630-1633.
    • (1999) Arch Ophthalmol , vol.117 , pp. 1630-1633
    • Mellott, M.L.1    Brown, J.J.2    Fingert, J.H.3    Taylor, C.M.4    Keech, R.V.5    Sheffield, V.C.6
  • 5
  • 6
    • 84862250745 scopus 로고    scopus 로고
    • A novel locus for autosomal dominant congenital motornystagmus mapped to 1q31-q32.2 between D1S2816 and D1S2692
    • Xiao X, Li S, Guo X, Zhang Q. A novel locus for autosomal dominant congenital motornystagmus mapped to 1q31-q32.2 between D1S2816 and D1S2692. Hum Genet 2012; 131: 697-702.
    • (2012) Hum Genet , vol.131 , pp. 697-702
    • Xiao, X.1    Li, S.2    Guo, X.3    Zhang, Q.4
  • 7
    • 31544452824 scopus 로고    scopus 로고
    • Linkage analysis of two families with X-linked recessive congenital motor nystagmus
    • Guo X, Li S, Jia X, Xiao X, Wang P, Zhang Q. Linkage analysis of two families with X-linked recessive congenital motor nystagmus. J Hum Genet 2006; 51: 76-80.
    • (2006) J Hum Genet , vol.51 , pp. 76-80
    • Guo, X.1    Li, S.2    Jia, X.3    Xiao, X.4    Wang, P.5    Zhang, Q.6
  • 8
    • 34748825561 scopus 로고    scopus 로고
    • Novel mutations of the FRMD7 gene in X-linked congenital motor nystagmus
    • Zhang B, Liu Z, Zhao G etal. Novel mutations of the FRMD7 gene in X-linked congenital motor nystagmus. Mol Vis 2007; 13: 1674-1679.
    • (2007) Mol Vis , vol.13 , pp. 1674-1679
    • Zhang, B.1    Liu, Z.2    Zhao, G.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.