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Volumn 42, Issue 11, 2001, Pages 2728-2736

Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CLINICAL ARTICLE; ELECTRORETINOGRAM; GAP JUNCTION; GENE MUTATION; HUMAN; NIGHT BLINDNESS; PRIORITY JOURNAL; RETINA BIPOLAR GANGLION CELL; RETINA CONE; RETINA ROD;

EID: 0034799576     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (34)

References (59)
  • 15
    • 0033762779 scopus 로고    scopus 로고
    • The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein
    • (2000) Nat Genet , vol.26 , pp. 324-327
    • Pusch, C.M.1    Zeitz, C.2    Brandau, O.3
  • 41
    • 0017364372 scopus 로고
    • The organization of the outer plexiform layer in the retina of the cat: Electron microscopy observations
    • (1977) J Neurocytol , vol.6 , pp. 131-153
    • Kolb, H.1
  • 42
    • 0017594684 scopus 로고
    • Cat cones have rod input: A comparison of the response properties of cone-horizontal cell bodies in the retina of the cat
    • (1977) J Comp Neurol , vol.172 , pp. 109-136
    • Nelson, R.1
  • 50
    • 0028106167 scopus 로고
    • Current source density analysis of retinal field potentials. II: Pharmacological analysis of the b-wave and M-wave
    • (1994) J Neurophysiol , vol.72 , pp. 96-105
    • Xu, X.1    Karwoski, C.J.2
  • 53
    • 0025813482 scopus 로고
    • Low-frequency component of the photopic ERG in patients with X-linked congenital stationary blindness with myopia
    • (1991) Clin Vision Sci , vol.6 , pp. 309-315
    • Young, R.S.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.