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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Main Authors: | Elin L. Strachan, Delphi Mac White-Begg, John Crean, Alison L. Reynolds, Breandán N. Kennedy, Niamh C. O’Sullivan |
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Format: | article |
Language: | EN |
Published: |
Frontiers Media S.A.
2021
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Online Access: | https://doaj.org/article/62a7a2f1465a45b2b8fba7939ca5df29 |
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