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Our results demonstrate that GNAT2 is the third gene implicated in achromatopsia.
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We describe a patient with persistent cerebral achromatopsia occurring after bilateral occipital strokes.
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The vision in typical complete achromatopsia is mediated only by rods.
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Conclusion: We report the occurrence of CNGB3-achromatopsia in a new canine breed, the MAS.
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Patients with cerebral achromatopsia are commonly said to suffer due to their disturbed colour sense.
1
He will find that he has not given exactly the proper curves to secure achromatism.
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This artifice is specially adopted in objectives for astronomical photography (''pure actinic achromatism'').
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Soc., 1878), the most suitable for visual instruments (''optical achromatism,').
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The absence of this error is termed achromatism, and an optical system so corrected is termed achromatic.
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As the diameter of the lens was so small in comparison with its focal length, its want of achromatism was inappreciable.
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We have performed linkage analysis in eight families with rod monochromacy, an autosomal recessively inherited condition with complete color blindness.
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This defines an interval of approximately 3 cM covering the ACHM2 locus for rod monochromacy.
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Go into this then choose Simulate color space and Monochromacy to go gray.