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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...

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Bibliografiska uppgifter
Huvudupphovsmän: Conley, Shannon M., Naash, Muna I.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Cold Spring Harbor Laboratory Press 2014
Ämnen:
Länkar: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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