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Mutations in the splicing regulator Prp31 lead to retinal degeneration in Drosophila
Retinitis pigmentosa (RP) is a clinically heterogeneous disease affecting 1.6 million people worldwide. The second-largest group of genes causing autosomal dominant RP in human encodes regulators of the splicing machinery. Yet, how defects in splicing factor genes are linked to the aetiology of the...
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| Veröffentlicht in: | Biol Open |
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| Hauptverfasser: | , , , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
The Company of Biologists Ltd
2021
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7860132/ https://ncbi.nlm.nih.gov/pubmed/33495354 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/bio.052332 |
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