Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II-Reference-Cited by-同舟云学术

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Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II

Published:2006-02-28 Issue:10 Volume:103 Page:3764-3769
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Foulquier F.,Vasile E.,Schollen E.,Callewaert N.,Raemaekers T.,Quelhas D.,Jaeken J.,Mills P.,Winchester B.,Krieger M.,Annaert W.,Matthijs G.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference30 articles.

1. Congenital Disorders of Glycosylation: A Review

2. Congenital disorders of glycosylation (CDG): It's all in it!

3. Congenital Disorders of Glycosylation

4. Microheterogeneity of human serum transferrin: A biological phenomenon studied by isoelectric focusing in immobilized pH gradients

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