Serum N-glycan and O-glycan analysis by mass spectrometry for diagnosis of congenital disorders of glycosylation
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference19 articles.
1. Congenital disorders of glycosylation (CDG): it’s (nearly) all in it!;Jaeken;J. Inherit. Metab. Dis.,2011
2. The congenital disorders of glycosylation;He,2012
3. A novel congenital disorder of glycosylation type without central nervous system involvement caused by mutations in the phosphoglucomutase 1 gene;Perez;J. Inherit. Metab. Dis.,2013
4. Cryptogenic liver disease in four children: a novel congenital disorder of glycosylation;Mandato;Pediatr. Res.,2006
5. Comparison of the methods for profiling glycoprotein glycans—HUPO Human Disease Glycomics/Proteome Initiative multi-institutional study;Wada;Glycobiology,2007
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