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...
Enregistré dans:
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
|
Sujets: | |
Accès en ligne: | https://doaj.org/article/62a7a2f1465a45b2b8fba7939ca5df29 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|
Documents similaires
-
A transgenic zebrafish model for in vivo long-term imaging of retinotectal synaptogenesis
par: Xu-fei Du, et autres
Publié: (2018) -
Corrigendum: Retinal Organoids: Cultivation, Differentiation, and Transplantation
par: Xuying Li, et autres
Publié: (2021) -
Retinal Organoids: Cultivation, Differentiation, and Transplantation
par: Xuying Li, et autres
Publié: (2021) -
Number and Topographical Distribution of Retinal Ganglion Cells in Diurnal and Nocturnal Raptors
par: Coli,Alessandra, et autres
Publié: (2018) -
Effects of Monocular Deprivation on the Dendritic Features of Retinal Ganglion Cells
par: Mwachaka,Philip, et autres
Publié: (2014)