I. Audo, K. M. Bujakowska, T. Léveillard, S. Mohand-saïd, M. Lancelot et al., Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases, Orphanet Journal of Rare Diseases, vol.7, issue.1, 2012.
DOI : 10.1016/S0002-9394(01)00838-8

URL : https://hal.archives-ouvertes.fr/inserm-00697616

N. Mollema and N. B. Haider, Focus on Molecules: Nuclear hormone receptor Nr2e3: Impact on retinal development and disease, Experimental Eye Research, vol.91, issue.2, pp.116-117, 2010.
DOI : 10.1016/j.exer.2010.04.013

S. Reichman, A. Terray, A. Slembrouck, C. Nanteau, G. Orieux et al., From confluent human iPS cells to self-forming neural retina and retinal pigmented epithelium, Proceedings of the National Academy of Sciences, vol.8, issue.1, pp.8518-8523, 2014.
DOI : 10.1021/cb4001712

URL : http://www.pnas.org/content/111/23/8518.full.pdf

S. Reichman, A. Slembrouck, G. Gagliardi, A. Chaffiol, A. Terray et al., Generation of Storable Retinal Organoids and Retinal Pigmented Epithelium from Adherent Human iPS Cells in Xeno-Free and Feeder-Free Conditions, STEM CELLS, vol.10, issue.5, pp.1176-1188, 2017.
DOI : 10.2217/rme.15.1

URL : https://hal.archives-ouvertes.fr/hal-01480587

D. F. Schorderet and P. Escher, mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP), Human Mutation, vol.43, issue.11, pp.1475-1485, 2009.
DOI : 10.1001/archopht.1996.01100140158008

URL : http://onlinelibrary.wiley.com/doi/10.1002/humu.21096/pdf