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A Drosophila model to study retinitis pigmentosa pathology associated with mutations in the core splicing factor Prp8
Retinitis pigmentosa (RP) represents genetically heterogeneous and clinically variable disease characterized by progressive degeneration of photoreceptors resulting in a gradual loss of vision. The autosomal dominant RP type 13 (RP13) has been linked to the malfunction of PRPF8, an essential compone...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Company of Biologists Ltd
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7328144/ https://www.ncbi.nlm.nih.gov/pubmed/32424050 http://dx.doi.org/10.1242/dmm.043174 |