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Course of Ocular Function in PRPF31 Retinitis Pigmentosa
Mutations in pre-mRNA splicing factors are the second most common cause of autosomal dominant retinitis pigmentosa, and a major cause of vision loss [1–3]. The development of gene augmentation therapy for disease caused by mutations in PRPF31 necessitates defining pre-treatment characteristics and d...
Na minha lista:
| Foilsithe in: | Semin Ophthalmol |
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| Main Authors: | , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2016
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6377939/ https://ncbi.nlm.nih.gov/pubmed/26959129 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/08820538.2015.1114856 |
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