Cone Survival: Identification of RdCVF

Author:

Lorentz Olivier,Sahel José,Mohand-Saïd Saddek,Leveillard Thierry

Publisher

Springer US

Reference29 articles.

1. K. Kajiwara, E. L. Berson, and T. P. Dryja. Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci, Science. 264(5165):1604–8 (1994).

2. M. E. McLaughlin, M. A. Sandberg, E. L. Berson, and T. P. Dryja. Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa, Nat Genet. 4(2):130–4 (1993).

3. P. J. Rosenfeld, L. B. Hahn, M. A. Sandberg, T. P. Dryja, and E. L. Berson. Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutation, Invest Ophthalmol Vis Sci. 36(11):2186–92 (1995).

4. G. Q. Chang, Y. Hao, and F. Wong. Apoptosis: final common patxhway of photoreceptor death in rd, rds, and rhodopsin mutant mice, Neuron. 11(4):595–605 (1993).

5. L. D. Carter-Dawson, M. M. LaVail, and R. L. Sidman. Differential effect of the rd mutation on rods and cones in the mouse retina, Invest Ophthalmol Vis Sci. 17(6):489–98 (1978).

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