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Photoreceptor progenitor mRNA analysis reveals exon skipping resulting from the ABCA4 c.5461-10T/C mutation in Stargardt disease

(2016) OPHTHALMOLOGY. 123(6). p.1375-1385
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inherited blindness, induced pluripotent stem cells, Stargardt disease, MACULAR DEGENERATION, RETINITIS-PIGMENTOSA, RETINAL DYSTROPHIES, BIOCHEMICAL DEFECTS, SEQUENCE VARIATION, TRANSPORTER ABCA4, GENE, VARIANTS, EXPRESSION, POPULATION

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Citation

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Chicago
Sangermano, Riccardo, Nathalie M Bax, Miriam Bauwens, L Ingeborgh Van den Born, Elfride De Baere, Alejandro Garanto, Rob WJ Collin, et al. 2016. “Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T/C Mutation in Stargardt Disease.” Ophthalmology 123 (6): 1375–1385.
APA
Sangermano, R., Bax, N. M., Bauwens, M., Van den Born, L. I., De Baere, E., Garanto, A., Collin, R. W., et al. (2016). Photoreceptor progenitor mRNA analysis reveals exon skipping resulting from the ABCA4 c.5461-10T/C mutation in Stargardt disease. OPHTHALMOLOGY, 123(6), 1375–1385.
Vancouver
1.
Sangermano R, Bax NM, Bauwens M, Van den Born LI, De Baere E, Garanto A, et al. Photoreceptor progenitor mRNA analysis reveals exon skipping resulting from the ABCA4 c.5461-10T/C mutation in Stargardt disease. OPHTHALMOLOGY. 2016;123(6):1375–85.
MLA
Sangermano, Riccardo, Nathalie M Bax, Miriam Bauwens, et al. “Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T/C Mutation in Stargardt Disease.” OPHTHALMOLOGY 123.6 (2016): 1375–1385. Print.
@article{7106537,
  author       = {Sangermano, Riccardo and Bax, Nathalie M and Bauwens, Miriam and Van den Born, L Ingeborgh and De Baere, Elfride and Garanto, Alejandro and Collin, Rob WJ and Goercharn-Ramlal, Angelique SA and  den Engelsman-van Dijk, Anke HA and Rohrschneider, Klaus and Hoyng, Carel B and Cremers, Frans PM and Albert, Silvia},
  issn         = {0161-6420},
  journal      = {OPHTHALMOLOGY},
  keyword      = {inherited blindness,induced pluripotent stem cells,Stargardt disease,MACULAR DEGENERATION,RETINITIS-PIGMENTOSA,RETINAL DYSTROPHIES,BIOCHEMICAL DEFECTS,SEQUENCE VARIATION,TRANSPORTER ABCA4,GENE,VARIANTS,EXPRESSION,POPULATION},
  language     = {eng},
  number       = {6},
  pages        = {1375--1385},
  title        = {Photoreceptor progenitor mRNA analysis reveals exon skipping resulting from the ABCA4 c.5461-10T/C mutation in Stargardt disease},
  url          = {http://dx.doi.org/10.1016/j.ophtha.2016.01.053},
  volume       = {123},
  year         = {2016},
}

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