Golgi function and dysfunction in the first COG4-deficient CDG type II patient

The conserved oligomeric Golgi (COG) complex is a hetero-octameric complex essential for normal glycosylation and intra-Golgi transport. An increasing number of congenital disorder of glycosylation type II (CDG-II) mutations are found in COG subunits indicating its importance in glycosylation. We re...

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Main Authors: Reynders, Ellen, Foulquier, François, Leão Teles, Elisa, Quelhas, Dulce, Morelle, Willy, Rabouille, Cathérine, Annaert, Wim, Matthijs, Gert
Format: Artigo
Jezik:Inglês
Izdano: Oxford University Press 2009
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Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC2722986/
https://ncbi.nlm.nih.gov/pubmed/19494034
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp262
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