Author:
Van Schil Kristof,Karlstetter Marcus,Aslanidis Alexander,Dannhausen Katharina,Azam Maleeha,Qamar Raheel,Leroy Bart P.,Depasse Fanny,Langmann Thomas,De Baere Elfride
Publisher
Springer Science and Business Media LLC
Reference58 articles.
1. Hartong, D. T., Berson, E. L. & Dryja, T. P. Retinitis pigmentosa. Lancet 368, 1795–1809 (2006).
2. Daiger, S. P., Sullivan, L. S. & Bowne, S. J. Genes and mutations causing retinitis pigmentosa. Clin Genet. 84, 132–141 (2013).
3. Daiger, S. P., Sullivan, L. S., Bowne, S. J. & Rossiter, B. J. F. RetNet. Retinal Information Network. Date of access: 28/09/2015 at
https://sph.uth.edu/retnet/
(1996).
4. Dryja, T. P., Hahn, L. B., Cowley, G. S., Mcgee, T. L. & Berson, E. L. Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa. Proc Natl Acad Sci USA. 88, 9370–9374 (1991).
5. 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).
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