Protanopia

Author:

Paramei Galina V.,Bimler David L.

Publisher

Springer Berlin Heidelberg

Reference19 articles.

1. Sharpe, L.T., Stockman, A., Jägle, H., Nathans, J.: Opsin genes, cone pigments, color vision and colorblindness. In: Gegenfurtner, K., Sharpe, L.T. (eds.) Color Vision: from Genes to Perception, Ch. 1, pp. 3–52. Cambridge University Press, Cambridge (1999)

2. Carroll, J., Neitz, M., Hofer, H., Neitz, J., Williams, D.R.: Functional photoreceptor loss revealed with adaptive optics: an alternate cause of color blindness. Proc. Natl. Acad. Sci. U. S. A. 101, 8461–8466 (2004)

3. Neitz, M., Neitz, M.: The genetics of normal and defective color vision. Vis. Res. 51, 633–651 (2011)

4. Hunt, D.M., Carvalho, L.S.: The genetics of color vision and congenial color deficiencies. In: Kremers, J., Baraas, R.C., Marshall, N.J. (eds.) Human Color Vision, Ch. 1, pp. 1–32. Springer, Cham (2016)

5. Jordan, G., Mollon, J.D.: A study of women heterozygous for colour deficiencies. Vis. Res. 33, 1495–1508 (1993)

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