Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) Causes a Novel Congenital Disorder of Glycosylation Type Ij-Reference-Cited by-同舟云学术

Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) Causes a Novel Congenital Disorder of Glycosylation Type Ij

Published:2003-07-14 Issue:2 Volume:22 Page:144-150
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Wu Xiaohua,Rush Jeffrey S.,Karaoglu Denise,Krasnewich Donna,Lubinsky Mark S.,Waechter Charles J.,Gilmore Reid,Freeze Hudson H.

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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