Molecular mechanisms underlying inherited photoreceptor degeneration as targets for therapeutic intervention
Retinitis pigmentosa (RP) is a form of retinal degeneration characterized by primary degeneration of rod photoreceptors followed by a secondary cone loss that leads to vision impairment and finally blindness. This is a rare disease with mutations in several genes and high genetic heterogeneity. A ch...
| Published in: | Frontiers in Cellular Neuroscience |
|---|---|
| Main Authors: | , , , , |
| Format: | Article |
| Language: | English |
| Published: |
Frontiers Media S.A.
2024-02-01
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| Subjects: | |
| Online Access: | https://www.frontiersin.org/articles/10.3389/fncel.2024.1343544/full |
