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Middle Wavelength Sensitive Photopigment Gene Expression is Absent in Deuteranomalous Colour Vision

Neitz, Maureen, Bollinger, Kathryn, Neitz, Jay·2003·Normal and Defective Colour Vision
DOI 10.1093/acprof:oso/9780198525301.003.0033
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Abstract

The deutan-type colour vision deficiencies, deuteranopia, and deuteranomaly are the most common types of colour blindness. A known cause of deutan colour vision defects is the loss of genes encoding the middle wavelength sensitive (M) photopigments. Deutan defects have also been found to be associated with a deleterious point mutation in the M photopigment genes. This chapter tests the hypothesis that M gene expression is absent in all commonly occurring deutan defects. It shows that the commonly occurring deutan defects in which individuals have normal appearing M genes, are caused by a failure to express M pigment. Moreover, it appears that the failure is likely to be complete.

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Research works printed but not linked: 26

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Metadata

Authors
Neitz, M., Bollinger, K., & Neitz, J.
Venue
Normal and Defective Colour Vision
Publisher
Oxford University PressOxford
Published
2003-05-08
Pages
318-328
DOI
10.1093/acprof:oso/9780198525301.003.0033
Cited by
3
References
0
Language
en

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