A New Preclinical Model of Retinitis Pigmentosa Due to Pde6g Deficiency
Purpose: Retinitis pigmentosa (RP) is the most common cause of inherited blindness, with onset occurring as early as 4 years of age in certain rare but severe forms caused by mutations in the gamma subunit of phosphodiesterase 6 (PDE6). Studies in humans and mice have shown that RP pathology begins...
| Glavni autori: | , , |
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| Format: | Članak |
| Jezik: | English |
| Izdano: |
Elsevier
2023-12-01
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| Serija: | Ophthalmology Science |
| Teme: | |
| Online pristup: | http://www.sciencedirect.com/science/article/pii/S2666914523000647 |