Structural changes to primary visual cortex in the congenital absence of cone input in achromatopsia

Structural changes to primary visual cortex in the congenital absence of cone input in achromatopsia

Autosomal recessive Achromatopsia (ACHM) is a rare inherited disorder associated with dysfunctional cone photoreceptors resulting in a congenital absence of cone input to visual cortex. This might lead to distinct changes in cortical architecture with a negative impact on the success of gene augment...

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Bibliographic Details
Main Authors: Barbara Molz, Anne Herbik, Heidi A. Baseler, Pieter B. de Best, Richard W. Vernon, Noa Raz, Andre D. Gouws, Khazar Ahmadi, Rebecca Lowndes, Rebecca J. McLean, Irene Gottlob, Susanne Kohl, Lars Choritz, John Maguire, Martin Kanowski, Barbara Käsmann-Kellner, Ilse Wieland, Eyal Banin, Netta Levin, Michael B. Hoffmann, Antony B. Morland
Format: Article
Language:English
Published: Elsevier 2022-01-01
Series:NeuroImage: Clinical
Subjects:
Achromatopsia
sMRI
Surface-based morphology
Plasticity
Primary visual cortex
Online Access:http://www.sciencedirect.com/science/article/pii/S2213158221003697

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