Defects in the assembly of dolichol-linked oligosaccharide or its transfer to proteins result in severe, multi-system human diseases called Type I congenital disorders of glycosylation. We have identified a novel CDG type, CDG-Ij, resulting from deficiency in UDP-GlcNAc: dolichol phosphate N-acetyl-
β¦ LIBER β¦
Mechanism of action of tunicamycin on the UDP-GlcNAc:dolichyl-phosphate GlcNAc-1-phosphate transferase
β Scribed by Heifetz, Aaron; Keenan, Roy W.; Elbein, Alan D.
- Book ID
- 126436322
- Publisher
- American Chemical Society
- Year
- 1979
- Tongue
- English
- Weight
- 872 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0006-2960
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