Title : Analysis of congenital disorder of glycosylation-Id in a yeast model system shows diverse site-specific under-glycosylation of glycoproteins.

Pub. Date : 2012 Nov 2

PMID : 23038983






2 Functional Relationships(s)
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Sentence
Compound Name
Protein Name
Organism
1 Mutations in the human ALG3 gene cause changed levels and altered glycan structures on mature glycoproteins and are the cause of a severe congenital disorder of glycosylation (CDG-Id). Polysaccharides ALG3 alpha-1,3- mannosyltransferase Homo sapiens
2 Mutations in the human ALG3 gene cause changed levels and altered glycan structures on mature glycoproteins and are the cause of a severe congenital disorder of glycosylation (CDG-Id). cdg ALG3 alpha-1,3- mannosyltransferase Homo sapiens