Загрузка...
Lack of Overt Retinal Degeneration in a K42E Dhdds Knock-In Mouse Model of RP59
Dehydrodolichyl diphosphate synthase (DHDDS) is required for protein N-glycosylation in eukaryotic cells. A K42E point mutation in the DHDDS gene causes an autosomal recessive form of retinitis pigmentosa (RP59), which has been classified as a congenital disease of glycosylation (CDG). We generated...
Сохранить в:
| Опубликовано в: : | Cells |
|---|---|
| Главные авторы: | , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
MDPI
2020
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7226774/ https://ncbi.nlm.nih.gov/pubmed/32272552 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/cells9040896 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|