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...

Descripción completa

Detalles Bibliográficos
Autores principales: Stanković, Dimitrije, Claudius, Ann-Katrin, Schertel, Thomas, Bresser, Tina, Uhlirova, Mirka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2020
Materias:
Research Article
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

Internet

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

Ejemplares similares