Structural Differences Across Multiple Visual Cortical Regions in the Absence of Cone Function in Congenital Achromatopsia

Most individuals with congenital achromatopsia (ACHM) carry mutations that affect the retinal phototransduction pathway of cone photoreceptors, fundamental to both high acuity vision and colour perception. As the central fovea is occupied solely by cones, achromats have an absence of retinal input t...

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Bibliographic Details
Published in:Frontiers in neuroscience Vol. 15; p. 718958
Main Authors: Lowndes, Rebecca, Molz, Barbara, Warriner, Lucy, Herbik, Anne, de Best, Pieter B., Raz, Noa, Gouws, Andre, Ahmadi, Khazar, McLean, Rebecca J., Gottlob, Irene, Kohl, Susanne, Choritz, Lars, Maguire, John, Kanowski, Martin, Käsmann-Kellner, Barbara, Wieland, Ilse, Banin, Eyal, Levin, Netta, Hoffmann, Michael B., Morland, Antony B., Baseler, Heidi A.
Format: Journal Article
Language:English
Published: Switzerland Frontiers Media S.A 14.10.2021
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ISSN:1662-453X, 1662-4548, 1662-453X
Online Access:Get full text
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