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Variations in opsin coding sequences cause x-linked cone dysfunction syndrome with myopia and dichromacy.
Invest Ophthalmol Vis Sci. 2013 Feb 15;54(2):1361-9. doi: 10.1167/iovs.12-11156.
Invest Ophthalmol Vis Sci. 2013.
PMID: 23322568
Free PMC article.
X-linked cone dystrophy and colour vision deficiency arising from a missense mutation in a hybrid L/M cone opsin gene.
McClements M, Davies WI, Michaelides M, Carroll J, Rha J, Mollon JD, Neitz M, MacLaren RE, Moore AT, Hunt DM.
McClements M, et al.
Vision Res. 2013 Mar 22;80:41-50. doi: 10.1016/j.visres.2012.12.012. Epub 2013 Jan 18.
Vision Res. 2013.
PMID: 23337435
Free PMC article.
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