Vertebrate Animal Models of RP59: Current Status and Future Prospects

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 <i>NUS1</i>) to form a <i>cis</i>-prenyltransferase (...

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Bibliographic Details
Main Authors: Steven J. Fliesler, Sriganesh Ramachandra Rao, Mai N. Nguyen, Mahmoud Tawfik KhalafAllah, Steven J. Pittler
Format: Article
Language:English
Published: MDPI AG 2022-11-01
Series:International Journal of Molecular Sciences
Subjects:
<i>cis</i>-prenyltransferase
DHDDS
dolichol
nogo-B receptor
retinal degeneration
RP59
Online Access:https://www.mdpi.com/1422-0067/23/21/13324

Internet

https://www.mdpi.com/1422-0067/23/21/13324

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