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The spectrum of ocular phenotypes caused by mutations in the BEST1 gene

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Keywords
AUTOSOMAL-DOMINANT VITREORETINOCHOROIDOPATHY, CHOROIDAL NEOVASCULAR MEMBRANE, VITELLIFORM MACULAR DYSTROPHY, RETINAL-PIGMENT EPITHELIUM, OPTICAL COHERENCE TOMOGRAPHY, Bestrophin-1, Best vitelliform macular dystrophy, FUNDUS AUTOFLUORESCENCE, ROD-CONE DYSTROPHY, BASAL LAMINAR DRUSEN, BEST1, Adult-onset foveomacular vitelliform, dystrophy, vitreoretinochoroidopathy, Autosomal dominant, Autosomal recessive bestrophinopathy, VMD2 GENE, Genotype-phenotype correlation, LIGHT-INDUCED DAMAGE

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Citation

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Chicago
Boon, Camiel JF, B Jeroen Klevering, Bart Leroy, Carel B Hoyng, Jan EE Keunen, and Anneke I den Hollander. 2009. “The Spectrum of Ocular Phenotypes Caused by Mutations in the BEST1 Gene.” Progress in Retinal and Eye Research 28 (3): 187–205.
APA
Boon, C. J., Klevering, B. J., Leroy, B., Hoyng, C. B., Keunen, J. E., & den Hollander, A. I. (2009). The spectrum of ocular phenotypes caused by mutations in the BEST1 gene. PROGRESS IN RETINAL AND EYE RESEARCH, 28(3), 187–205.
Vancouver
1.
Boon CJ, Klevering BJ, Leroy B, Hoyng CB, Keunen JE, den Hollander AI. The spectrum of ocular phenotypes caused by mutations in the BEST1 gene. PROGRESS IN RETINAL AND EYE RESEARCH. 2009;28(3):187–205.
MLA
Boon, Camiel JF et al. “The Spectrum of Ocular Phenotypes Caused by Mutations in the BEST1 Gene.” PROGRESS IN RETINAL AND EYE RESEARCH 28.3 (2009): 187–205. Print.
@article{940954,
  author       = {Boon, Camiel JF and Klevering, B Jeroen and Leroy, Bart and Hoyng, Carel B and Keunen, Jan EE and den Hollander, Anneke I},
  issn         = {1350-9462},
  journal      = {PROGRESS IN RETINAL AND EYE RESEARCH},
  keywords     = {AUTOSOMAL-DOMINANT VITREORETINOCHOROIDOPATHY,CHOROIDAL NEOVASCULAR MEMBRANE,VITELLIFORM MACULAR DYSTROPHY,RETINAL-PIGMENT EPITHELIUM,OPTICAL COHERENCE TOMOGRAPHY,Bestrophin-1,Best vitelliform macular dystrophy,FUNDUS AUTOFLUORESCENCE,ROD-CONE DYSTROPHY,BASAL LAMINAR DRUSEN,BEST1,Adult-onset foveomacular vitelliform,dystrophy,vitreoretinochoroidopathy,Autosomal dominant,Autosomal recessive bestrophinopathy,VMD2 GENE,Genotype-phenotype correlation,LIGHT-INDUCED DAMAGE},
  language     = {eng},
  number       = {3},
  pages        = {187--205},
  title        = {The spectrum of ocular phenotypes caused by mutations in the BEST1 gene},
  url          = {http://dx.doi.org/10.1016/j.preteyeres.2009.04.002},
  volume       = {28},
  year         = {2009},
}

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