Retinal fingerprints of ALS in patients: Ganglion cell apoptosis and TDP-43/p62 misplacement
IntroductionAmyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease characterized by the progressive loss of motor neuron function. Although ophthalmic deficits are not considered a classic symptom of ALS, recent studies suggest that changes in retinal cells, similar to those in the...
Збережено в:
| Автори: | , , , , , , , |
|---|---|
| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Frontiers Media S.A.
2023-03-01
|
| Серія: | Frontiers in Aging Neuroscience |
| Предмети: | |
| Онлайн доступ: | https://www.frontiersin.org/articles/10.3389/fnagi.2023.1110520/full |
| Теги: |
Немає тегів, Будьте першим, хто поставить тег для цього запису!
|