Testing for Congenital Disorders of Glycosylation by HPLC Measurement of Serum Transferrin Glycoforms
Author:
Affiliation:
1. Department of Clinical Neuroscience, Karolinska Institutet and University Hospital, Stockholm, Sweden
2. Glycobiology and Carbohydrate Chemistry Program, The Burnham Institute, La Jolla, CA
Publisher
Oxford University Press (OUP)
Subject
Biochemistry (medical),Clinical Biochemistry
Link
http://academic.oup.com/clinchem/article-pdf/50/5/954/32733032/clinchem0954.pdf
Reference21 articles.
1. Congenital disorders of glycosylation (CDG): It's all in it!
2. Congenital disorders of glycosylation: review of their molecular bases, clinical presentations and specific therapies
3. A New Type of Congenital Disorders of Glycosylation (CDG-Ii) Provides New Insights into the Early Steps of Dolichol-linked Oligosaccharide Biosynthesis
4. Deficiency of UDP-GlcNAc:Dolichol Phosphate N-Acetylglucosamine-1 Phosphate Transferase (DPAGT1) Causes a Novel Congenital Disorder of Glycosylation Type Ij
5. Deficiency of GDP-Man:GlcNAc2-PP-Dolichol Mannosyltransferase Causes Congenital Disorder of Glycosylation Type Ik
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