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Graefe's Archive for Clinical and Experimental Ophthalmology
Volumn 247, Issue 11, 2009, Pages 1561-1563
Shortening of the rod outer segment in Oguchi disease
Author keywords

[No Author keywords available]
Indexed keywords

ADULT; CASE REPORT; ELECTRORETINOGRAM; GENE MUTATION; HUMAN; LETTER; MALE; OGUCHI DISEASE; OPHTHALMOSCOPY; OPTICAL COHERENCE TOMOGRAPHY; OSCILLATORY POTENTIAL; PERIMETRY; PHOTORECEPTOR; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA ROD OUTER SEGMENT; RETINITIS PIGMENTOSA; VISUAL ACUITY; VISUAL FIELD;
EID: 70349859876     PISSN: 0721832X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00417-009-1114-6     Document Type: Letter
Times cited : (17)
References (5)
  • 2
    • 33845187792 scopus 로고    scopus 로고
    • Ultra-high resolution optical coherence tomography assessment of photoreceptors in retinitis pigmentosa and related diseases
    • doi: 10.1016/j.ajo.2006.07.024
    • Witkin AJ, Ko TH, Fujimoto JG, Chan A, Drexler W, Schuman JS, Reichel E, Duker JS (2006) Ultra-high resolution optical coherence tomography assessment of photoreceptors in retinitis pigmentosa and related diseases. Am J Ophthalmol 142:945-952. doi: 10.1016/j.ajo.2006.07.024
    • (2006) Am J Ophthalmol , vol.142 , pp. 945-952
    • Witkin, A.J.1    Ko, T.H.2    Fujimoto, J.G.3    Chan, A.4    Drexler, W.5    Schuman, J.S.6    Reichel, E.7    Duker, J.S.8
  • 3
    • 0029067542 scopus 로고
    • A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese
    • doi: 10.1038/ng0795-360
    • Fuchs S, Nakazawa M, Maw M, Tamai M, Oguchi Y, Gal A (1995) A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese. Nat Genet 10:360-362. doi: 10.1038/ng0795-360
    • (1995) Nat Genet , vol.10 , pp. 360-362
    • Fuchs, S.1    Nakazawa, M.2    Maw, M.3    Tamai, M.4    Oguchi, Y.5    Gal, A.6
  • 4
    • 0031038950 scopus 로고    scopus 로고
    • Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness
    • doi: 10.1038/ng0297-175
    • Yamamoto S, Sipple KC, Berson EL, Dryja TP (1997) Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness. Nat Genet 15:175-178. doi: 10.1038/ng0297-175
    • (1997) Nat Genet , vol.15 , pp. 175-178
    • Yamamoto, S.1    Sipple, K.C.2    Berson, E.L.3    Dryja, T.P.4
  • 5
    • 8244231270 scopus 로고    scopus 로고
    • The Mizuo phenomenon in Oguchi disease
    • Bergsma DR Jr, Chen CJ (1997) The Mizuo phenomenon in Oguchi disease. Arch Ophthalmol 115:560-561
    • (1997) Arch Ophthalmol , vol.115 , pp. 560-561
    • Bergsma Jr., D.R.1    Chen, C.J.2

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.