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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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Keywords
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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MLA
Sangermano, Riccardo, et al. “Photoreceptor Progenitor MRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T/C Mutation in Stargardt Disease.” OPHTHALMOLOGY, vol. 123, no. 6, 2016, pp. 1375–85.
APA
Sangermano, R., Bax, N. M., Bauwens, M., Van den Born, L. I., De Baere, E., Garanto, A., … Albert, S. (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.
Chicago author-date
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): 1375–85.
Chicago author-date (all authors)
Sangermano, Riccardo, Nathalie M Bax, Miriam Bauwens, L Ingeborgh Van den Born, Elfride De Baere, Alejandro Garanto, Rob WJ Collin, Angelique SA Goercharn-Ramlal, Anke HA den Engelsman-van Dijk, Klaus Rohrschneider, Carel B Hoyng, Frans PM Cremers, and Silvia Albert. 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.
IEEE
[1]
R. Sangermano et al., “Photoreceptor progenitor mRNA analysis reveals exon skipping resulting from the ABCA4 c.5461-10T/C mutation in Stargardt disease,” OPHTHALMOLOGY, vol. 123, no. 6, pp. 1375–1385, 2016.
@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},
  keywords     = {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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