Defect in N-glycosylation of proteins is tissue-dependent in Congenital Disorders of Glycosylation Ia
Author:
Publisher
Oxford University Press (OUP)
Subject
Biochemistry
Link
http://academic.oup.com/glycob/article-pdf/10/12/1277/9806081/101277.pdf
Reference28 articles.
1. The role of N-glycosylation of GLUT1 for glucose transport activity.
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3. Carbohydrate-deficient glycoprotein syndrome: normal glycosylation in the fetus
4. Alteration of mannose transport in fibroblasts from type I carbohydrate deficient glycoprotein syndrome patients
5. β-Trace protein in human cerebrospinal fluid: a diagnostic marker for N-glycosylation defects in brain
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