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Ophthalmology
Volumn 121, Issue 3, 2014, Pages
CABP4 mutations do not cause congenital stationary night blindness
Author keywords

[No Author keywords available]
Indexed keywords

CALCIUM BINDING PROTEIN 4; PROTEIN; UNCLASSIFIED DRUG;
EID: 84896727718     PISSN: 01616420     EISSN: 15494713     Source Type: Journal    
DOI: 10.1016/j.ophtha.2013.11.005     Document Type: Letter
Times cited : (15)
References (4)
  • 1
    • 84885023333 scopus 로고    scopus 로고
    • Genotype and phenotype of 101 Dutch patients with congenital stationary night blindness
    • M.M. Bijveld, R.J. Florijn, and A.A. Bergen et al. Genotype and phenotype of 101 Dutch patients with congenital stationary night blindness Ophthalmology 120 2013 2072 2081
    • (2013) Ophthalmology , vol.120 , pp. 2072-2081
    • Bijveld, M.M.1    Florijn, R.J.2    Bergen, A.A.3
  • 2
    • 84874666704 scopus 로고    scopus 로고
    • Clinical characterisation of the CABP4-related retinal phenotype
    • A.O. Khan, M. Alrashed, and F.S. Alkuraya Clinical characterisation of the CABP4-related retinal phenotype Br J Ophthalmol 97 2013 262 265
    • (2013) Br J Ophthalmol , vol.97 , pp. 262-265
    • Khan, A.O.1    Alrashed, M.2    Alkuraya, F.S.3
  • 3
    • 65549105124 scopus 로고    scopus 로고
    • A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder
    • K.W. Littink, M.M. van Genderen, and R.W. Collin et al. A novel homozygous nonsense mutation in CABP4 causes congenital cone-rod synaptic disorder Invest Ophthalmol Vis Sci 50 2009 2344 2350
    • (2009) Invest Ophthalmol Vis Sci , vol.50 , pp. 2344-2350
    • Littink, K.W.1    Van Genderen, M.M.2    Collin, R.W.3
  • 4
    • 84874661243 scopus 로고    scopus 로고
    • Childhood retinal dystrophies: What's in a name?
    • E.I. Traboulsi Childhood retinal dystrophies: what's in a name? Br J Ophthalmol 97 2013 247
    • (2013) Br J Ophthalmol , vol.97 , pp. 247
    • Traboulsi, E.I.1

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.