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Topographical cone photopigment gene expression in deutan-type red–green color vision defects

Bollinger, Kathryn, Sjoberg, Stacy A., Neitz, Maureen, Neitz, Jay·2004·Vision Research

Abstract

Eye donors were identified who had X-chromosome photopigment gene arrays like those of living deuteranomalous men; the arrays contained two genes encoding long-wavelength sensitive (L) pigments as well as genes to encode middle-wavelength sensitive (M) photopigment. Ultrasensitive methods failed to detect the presence of M photopigment mRNA in the retinas of these deutan donors. This provides direct evidence that deuteranomaly is caused by the complete absence of M pigment mRNA. Additionally, for those eyes with mRNA corresponding to two different L-type photopigments, the ratio of mRNA from the first vs. downstream L genes was analyzed across the retinal topography. Results show that the pattern of first relative to downstream L gene expression in the deuteranomalous retina is similar to the pattern of L vs. M gene expression found in normal retinas.

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Crossref · 10.1016/j.visres.2003.09.006

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Research works printed but not linked: 33

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Metadata

Authors
Bollinger, K., Sjoberg, S. A., Neitz, M., & Neitz, J.
Venue
Vision Research
Publisher
Elsevier BV
Published
2004-01
Volume
44
Issue
2
Pages
135-145
ISSN
0042-6989
Cited by
11
References
0
Language
en

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CoChat. (2026). Citation check: Topographical cone photopigment gene expression in deutan-type red–green color vision defects. https://app.cochat.ai/papers/10.1016/j.visres.2003.09.006
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Bollinger, K., Sjoberg, S. A., Neitz, M., & Neitz, J. (2004). Topographical cone photopigment gene expression in deutan-type red–green color vision defects. Vision Research. https://doi.org/10.1016/j.visres.2003.09.006

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