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...

Full description

Saved in:
Bibliographic Details
Published in:Dis Model Mech
Main Authors: Stanković, Dimitrije, Claudius, Ann-Katrin, Schertel, Thomas, Bresser, Tina, Uhlirova, Mirka
Format: Artigo
Language:Inglês
Published: The Company of Biologists Ltd 2020
Subjects:
Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7328144/
https://ncbi.nlm.nih.gov/pubmed/32424050
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.043174
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items