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2.Baehr W, Frederick JM. Naturally occurring animal models with outer retina phenotypes. Vis Res,2009,49: 2636-2652

3.Bourne MC, Campbell DA, Tansley K. Hereditary degeneration of rat retina. Br J Ophthalmol, 1938,22(10): 613-623

4.Bundey S,Crews SJ. A study of retinitis pigrnentosa in the city of Birmingham-I. J Med Genet, 1984,21(6):417-420

5.Chang B, Heckenlively IB,Bayley PR.et a.I. The nob2 mouse, a null mutation in Cacnalf: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses. Vis Neurosci, 2006, 23 (1): 11-24

6.Criswell MH,Ciulla TA,Hill TE,et al. The squirrelmonkey: characterization of a new-world primate model of xperimental choroidal neovascularizalion and comparison with the macaque. Invest Ophthalmol Vis Sci,2004, 45 (2): 625-634

7.Gu Y, Wang L,Zhou J,et al. A naturally-occurring mutation in CacnaIf in a rat model of congenital stationary night blindness. Mo! Vis,2008, 14(1):20-28

8.Lue CL. Rod cell activity in retinal degenerative rats. J Formos Med Assoc, 1994,93(7):605-610

9.Pinkert CA. Transgenic animal technology. New York: Academic Press, 1994

10.Sato H, Suzuki T, Ikeda K, et aL A monogenic dominant mutation in Rom l generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice. Mol Vis,2010, 16:378-391

11.Williams TP, Howell WL. Action spectrum of retinal light-damage in albino rats. Invest Ophthalmol Vis Sci, 1983, 24 (3):285-287

12.Won J, Shi LY, Hicks W, et al. Mouse model resources for vision research. J Ophthalmol,2011,2011:391384

13.Xie B,Nakanishi S,Guo Q,et al. A novel middle­wavelength opsin (M-opsin) null-mutation in the retinal cone dysfunction ral. Exp Eye Res,2010,91(1):26-33

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2.Baehr W, Frederick JM. Naturally occurring animal models with outer retina phenotypes. Vis Res,2009,49: 2636-2652

3.Bourne MC, Campbell DA, Tansley K. Hereditary degeneration of rat retina. Br J Ophthalmol, 1938,22(10): 613-623

4.Bundey S,Crews SJ. A study of retinitis pigrnentosa in the city of Birmingham-I. J Med Genet, 1984,21(6):417-420

5.Chang B, Heckenlively IB,Bayley PR.et a.I. The nob2 mouse, a null mutation in Cacnalf: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responses. Vis Neurosci, 2006, 23 (1): 11-24

6.Criswell MH,Ciulla TA,Hill TE,et al. The squirrelmonkey: characterization of a new-world primate model of xperimental choroidal neovascularizalion and comparison with the macaque. Invest Ophthalmol Vis Sci,2004, 45 (2): 625-634

7.Gu Y, Wang L,Zhou J,et al. A naturally-occurring mutation in CacnaIf in a rat model of congenital stationary night blindness. Mo! Vis,2008, 14(1):20-28

8.Lue CL. Rod cell activity in retinal degenerative rats. J Formos Med Assoc, 1994,93(7):605-610

9.Pinkert CA. Transgenic animal technology. New York: Academic Press, 1994

10.Sato H, Suzuki T, Ikeda K, et aL A monogenic dominant mutation in Rom l generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice. Mol Vis,2010, 16:378-391

11.Williams TP, Howell WL. Action spectrum of retinal light-damage in albino rats. Invest Ophthalmol Vis Sci, 1983, 24 (3):285-287

12.Won J, Shi LY, Hicks W, et al. Mouse model resources for vision research. J Ophthalmol,2011,2011:391384

13.Xie B,Nakanishi S,Guo Q,et al. A novel middle­wavelength opsin (M-opsin) null-mutation in the retinal cone dysfunction ral. Exp Eye Res,2010,91(1):26-33

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