Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) Causes a Novel Congenital Disorder of Glycosylation Type Ij
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference29 articles.
1. A Deficiency in Dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl α3-Glucosyltransferase Defines a New Subtype of Congenital Disorders of Glycosylation
2. Conserved sequences in enzymes of the UDP-GlcNAc/MurNAc family are essential in hamster UDP-GlcNAc:dolichol-P GlcNAc-1-P transferase
3. Oligomerization of Hamster UDP-GlcNAc:Dolichol-P GlcNAc-1-P Transferase, an Enzyme with Multiple Transmembrane Spans
4. A simple procedure for preparing dolichyl monophosphate by the use of POCl3
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