Associated Papers
Inherited Retinal Degeneration Caused by Dehydrodolichyl Diphosphate Synthase Mutation-Effect of an ALG6 Modifier Variant.
Monson E et al.
International Journal of Molecular Sciences, 2024
A case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activity.
Sabry S et al.
Orphanet Journal of Rare Diseases, 2016
Select a paper to view details