A New Method for the Rapid Diagnosis of Protein N-linked Congenital Disorders of Glycosylation-Reference-Cited by-同舟云学术

A New Method for the Rapid Diagnosis of Protein N-linked Congenital Disorders of Glycosylation

Published:2013-06-17 Issue:7 Volume:12 Page:3471-3479
ISSN:1535-3893
Container-title:Journal of Proteome Research
language:en
Short-container-title:J. Proteome Res.

Author:

Heywood Wendy E.¹,Mills Philippa¹,Grunewald Stephanie¹²,Worthington Viki³,Jaeken Jaak⁴,Carreno Gabriela¹,Lemonde Hugh²,Clayton Peter T.¹,Mills Kevin¹

Affiliation:

1. Biochemistry Research Group, Clinical and Molecular Genetics Unit, Institute of Child Health & Great Ormond Street Hospital, University College London, United Kingdom

2. Great Ormond Street Hospital for Sick Children, Great Ormond Street, London WC1N 3JH, United Kingdom

3. Neuroimmunology & CSF Laboratory, Institute of Neurology, Queen Square London, WC1N 3BG, United Kingdom

4. Center for Metabolic Disease, University Hospital Gasthuisberg, Leuven, Belgium

Publisher

American Chemical Society (ACS)

Subject

General Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/pr400328g

Reference22 articles.

1. A Genetic Approach to Mammalian Glycan Function

2. On the frequency of protein glycosylation, as deduced from analysis of the SWISS-PROT database

3. Congenital disorders of glycosylation (CDG): it’s (nearly) all in it!

4. Congenital disorders of glycosylation

5. Glycomics of pediatric and adulthood diseases of the central nervous system

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