Congenital disorders of glycosylation: an update on defects affecting the biosynthesis of dolichol-linked oligosaccharides-Reference-Cited by-同舟云学术

Congenital disorders of glycosylation: an update on defects affecting the biosynthesis of dolichol-linked oligosaccharides

Published:2009-12 Issue:12 Volume:30 Page:1628-1641
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Haeuptle Micha A.,Hennet Thierry

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.21126/fullpdf

Reference124 articles.

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2. Requirement of the Lec35 gene for all known classes of monosaccharide-P-dolichol-dependent glycosyltransferase reactions in mammals;Anand;Mol Biol Cell,2001

3. Severe hypoglycemia as a presenting symptom of carbohydrate-deficient glycoprotein syndrome;Babovic-Vuksanovic;J Pediatr,1999

4. Biochemical and molecular studies in 26 Spanish patients with congenital disorder of glycosylation type Ia;Briones;J Inherit Metab Dis,2002

5. The ALG10 locus of Saccharomyces cerevisiae encodes the alpha-1,2 glucosyltransferase of the endoplasmic reticulum: the terminal glucose of the lipid-linked oligosaccharide is required for efficient N-linked glycosylation;Burda;Glycobiology,1998

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