Author:
Léveillard Thierry,Mohand-Saïd Saddek,Lorentz Olivier,Hicks David,Fintz Anne-Claire,Clérin Emmanuelle,Simonutti Manuel,Forster Valérie,Cavusoglu Nükhet,Chalmel Frédéric,Dollé Pascal,Poch Olivier,Lambrou George,Sahel José-Alain
Publisher
Springer Science and Business Media LLC
Reference21 articles.
1. Rosenfeld, P.J. et al. A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa. Nat. Genet. 1, 209–213 (1992).
2. McLaughlin, M.E., Sandberg, M.A., Berson, E.L. & Dryja, T.P. Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa. Nat. Genet. 4, 130–134 (1993).
3. Kajiwara, K., Berson, E.L. & Dryja, T.P. Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci. Science 264, 1604–1608 (1994).
4. Dowling, J.E. The retina: an approachable part of the brain. in Retinal Cells and Processing (Harvard University Press, Cambridge, Massachusetts, 1987).
5. Mohand-Saïd, S. et al. Photoreceptor transplants increase host cone survival in the retinal degeneration (rd) mouse. Ophthalmic Res. 29, 290–297 (1997).
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