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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Detalles Bibliográficos
Autores principales: Molz, Barbara, Herbik, Anne, Baseler, Heidi A., de Best, Pieter B., Vernon, Richard W., Raz, Noa, Gouws, Andre D., Ahmadi, Khazar, Lowndes, Rebecca, 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718719/
https://www.ncbi.nlm.nih.gov/pubmed/34959047
http://dx.doi.org/10.1016/j.nicl.2021.102925

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718719/
https://www.ncbi.nlm.nih.gov/pubmed/34959047
http://dx.doi.org/10.1016/j.nicl.2021.102925

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