Winderickx J; Sanocki E; Lindsey DT; et al. (1993). „Defective colour vision associated with a missense mutation in the human green visual pigment gene.”. Nat. Genet. 1 (4): 251—6. PMID1302020. doi:10.1038/ng0792-251.CS1 одржавање: Експлицитна употреба et al. (веза)
Neitz J, Neitz M, Jacobs GH (1990). „Analysis of fusion gene and encoded photopigment of colour-blind humans.”. Nature. 342 (6250): 679—82. PMID2574415. doi:10.1038/342679a0.
Nathans J, Thomas D, Hogness DS (1986). „Molecular genetics of human color vision: the genes encoding blue, green, and red pigments.”. Science. 232 (4747): 193—202. PMID2937147. doi:10.1126/science.2937147.
Li ZY, Kljavin IJ, Milam AH (1995). „Rod photoreceptor neurite sprouting in retinitis pigmentosa.”. J. Neurosci. 15 (8): 5429—38. PMID7643192.
Ferreira PA, Nakayama TA, Pak WL, Travis GH (1996). „Cyclophilin-related protein RanBP2 acts as chaperone for red/green opsin.”. Nature. 383 (6601): 637—40. PMID8857542. doi:10.1038/383637a0.
Bernstein SL, Wong P (1998). „Regional expression of disease-related genes in human and monkey retina.”. Mol. Vis. 4: 24. PMID9815288.
Hayashi T, Motulsky AG, Deeb SS (1999). „Position of a 'green-red' hybrid gene in the visual pigment array determines colour-vision phenotype.”. Nat. Genet. 22 (1): 90—3. PMID10319869. doi:10.1038/8798.
Ueyama H; Kuwayama S; Imai H; et al. (2002). „Novel missense mutations in red/green opsin genes in congenital color-vision deficiencies.”. Biochem. Biophys. Res. Commun. 294 (2): 205—9. PMID12051694. doi:10.1016/S0006-291X(02)00458-8.CS1 одржавање: Експлицитна употреба et al. (веза)
Zhu X; Brown B; Li A; et al. (2003). „GRK1-dependent phosphorylation of S and M opsins and their binding to cone arrestin during cone phototransduction in the mouse retina.”. J. Neurosci. 23 (14): 6152—60. PMID12853434.CS1 одржавање: Експлицитна употреба et al. (веза)
Bonilha VL, Hollyfield JG, Grover S, Fishman GA (2005). „Abnormal distribution of red/green cone opsins in a patient with an autosomal dominant cone dystrophy.”. Ophthalmic Genet. 26 (2): 69—76. PMID16020309. doi:10.1080/13816810590968041.