Color Blindness, Partial, Deutan Series (Deuteranopia) &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; &nbs 747c28h p; 270
General: Sex-linked; affects males; deuteranopes can have one red pigment gene and one anomalous hybrid red-green gene with a spectral absorbance close to the red pigment gene.
Ocular: Red-green color blindness.
Clinical: None.
Adam A, Fraser GR. The linkage between protan and deutan loci. Am J Hum Genet 1970; 22:691-693.
Boger WP III, Petersen RA. Pediatric Ophthalmology. Protan and deutan color blindness. In: Pavan-Langston D, ed. Manual of Ocular Diagnosis and Therapy, 4th ed. Boston: Little, Brown and Company, 1995:285-286.
McKusick VA. Mendelian Inheritance in Man; A Catalog of Human Genes and Genetic Disorders, 12th ed. Baltimore: The Johns Hopkins University Press, 1998.
Online Mendelian Inheritance in Man, OMIM. McKusick-Nathans Institute for Genetic Medicine, Johns Hopkins University and National Center for Biotechnology Information, National Library of Medicine, February 12, 2007. World Wide Web URL: https://www.ncbi.nlm.nih.gov/omim/.
Nathans J, et al. Molecular genetics of inherited variation in human color vision. Science 1986; 232:203-210.
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