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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Auteurs principaux: Elin L. Strachan, Delphi Mac White-Begg, John Crean, Alison L. Reynolds, Breandán N. Kennedy, Niamh C. O’Sullivan
Format: article
Langue:EN
Publié: Frontiers Media S.A. 2021
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Accès en ligne:https://doaj.org/article/62a7a2f1465a45b2b8fba7939ca5df29
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