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Volumn 109, Issue 3, 2002, Pages 575-583

A distinctive form of congenital stationary night blindness with cone ON-pathway dysfunction

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; B WAVE; CASE REPORT; COLOR VISION; DARK ADAPTATION; ELECTRORETINOGRAPHY; EVOKED VISUAL RESPONSE; GENE MUTATION; HUMAN; LIGHT DARK CYCLE; LUMINANCE; MALE; NIGHT BLINDNESS; PHOTORECEPTOR; PRIORITY JOURNAL; RETINA CONE; RETINA DISEASE; STIMULUS RESPONSE;

EID: 0036191219     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0161-6420(01)00981-2     Document Type: Article
Times cited : (32)

References (47)
  • 4
    • 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
  • 14
  • 25
    • 0028038981 scopus 로고
    • Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the β-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3
    • (1994) Hum Mol Genet , vol.3 , pp. 323-325
    • Gal, A.1    Xu, S.2    Piczenik, Y.3
  • 29
    • 0025813482 scopus 로고
    • Low-frequency component of the photopic ERG in patients with X-linked congenital stationary night blindness
    • (1991) Clin Vision Sci , vol.6 , pp. 309-315
    • Young, R.S.L.1
  • 47
    • 0028128535 scopus 로고
    • Heterozygous missense mutation in the rod cGMP phosphodiesterase β-subunit gene in autosomal dominant stationary night blindness
    • (1994) Nat Genet , vol.7 , pp. 64-68
    • Gal, A.1    Orth, U.2    Baehr, W.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.