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Gene Therapy for PRPH2-Associated Ocular Disease: Challenges and Prospects
The peripherin-2 (PRPH2) gene encodes a photoreceptor-specific tetraspanin protein called peripherin-2/retinal degeneration slow (RDS), which is critical for the formation and maintenance of rod and cone outer segments. Over 90 different disease-causing mutations in PRPH2 have been identified, which...
Tallennettuna:
| Päätekijät: | , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Cold Spring Harbor Laboratory Press
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4208711/ https://ncbi.nlm.nih.gov/pubmed/25167981 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a017376 |
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