The Role of Mitochondria in Optic Atrophy With Autosomal Inheritance

Optic atrophy (OA) with autosomal inheritance is a form of optic neuropathy characterized by the progressive and irreversible loss of vision. In some cases, this is accompanied by additional, typically neurological, extra-ocular symptoms. Underlying the loss of vision is the specific degeneration of...

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Detalles Bibliográficos
Autores principales: Strachan, Elin L., Mac White-Begg, Delphi, Crean, John, Reynolds, Alison L., Kennedy, Breandán N., O’Sullivan, Niamh C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634724/
https://www.ncbi.nlm.nih.gov/pubmed/34867178
http://dx.doi.org/10.3389/fnins.2021.784987

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634724/
https://www.ncbi.nlm.nih.gov/pubmed/34867178
http://dx.doi.org/10.3389/fnins.2021.784987

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