Vertebrate Animal Models of RP59: Current Status and Future Prospects

Retinitis pigmentosa-59 (RP59) is a rare, recessive form of RP, caused by mutations in the gene encoding DHDDS (dehydrodolichyl diphosphate synthase). DHDDS forms a heterotetrameric complex with Nogo-B receptor (NgBR; gene NUS1) to form a cis-prenyltransferase (CPT) enzyme complex, which is required...

Descripción completa

Detalles Bibliográficos
Autores principales: Fliesler, Steven J., Ramachandra Rao, Sriganesh, Nguyen, Mai N., KhalafAllah, Mahmoud Tawfik, Pittler, Steven J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9657489/
https://www.ncbi.nlm.nih.gov/pubmed/36362109
http://dx.doi.org/10.3390/ijms232113324

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9657489/
https://www.ncbi.nlm.nih.gov/pubmed/36362109
http://dx.doi.org/10.3390/ijms232113324

Ejemplares similares