Associated Papers
Reduced expression of the oligosaccharyltransferase exacerbates protein hypoglycosylation in cells lacking the fully assembled oligosaccharide donor.
Shrimal S et al.
Glycobiology, 2015
ALG6-CDG in South Africa: Genotype-Phenotype Description of Five Novel Patients.
Dercksen M et al.
Jimd Reports, 2013
Identification of a frequent variant in ALG6, the cause of Congenital Disorder of Glycosylation-Ic.
Westphal V et al.
Human Mutation, 2003
Reduced heparan sulfate accumulation in enterocytes contributes to protein-losing enteropathy in a congenital disorder of glycosylation.
Westphal V et al.
The American Journal of Pathology, 2000
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