Non-Image-Forming Light Driven Functions Are Preserved in a Mouse Model of Autosomal Dominant Optic Atrophy

Autosomal dominant optic atrophy (ADOA) is a slowly progressive optic neuropathy that has been associated with mutations of the OPA1 gene. In patients, the disease primarily affects the retinal ganglion cells (RGCs) and causes optic nerve atrophy and visual loss. A subset of RGCs are intrinsically p...

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Detalles Bibliográficos
Autores principales: Perganta, Georgia, Barnard, Alun R., Katti, Christiana, Vachtsevanos, Athanasios, Douglas, Ron H., MacLaren, Robert E., Votruba, Marcela, Sekaran, Sumathi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569441/
https://www.ncbi.nlm.nih.gov/pubmed/23409176
http://dx.doi.org/10.1371/journal.pone.0056350

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569441/
https://www.ncbi.nlm.nih.gov/pubmed/23409176
http://dx.doi.org/10.1371/journal.pone.0056350

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