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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Detalles Bibliográficos
Autores principales: Reynders, Ellen, Foulquier, François, Leão Teles, Elisa, Quelhas, Dulce, Morelle, Willy, Rabouille, Cathérine, Annaert, Wim, Matthijs, Gert
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2009
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722986/
https://www.ncbi.nlm.nih.gov/pubmed/19494034
http://dx.doi.org/10.1093/hmg/ddp262

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722986/
https://www.ncbi.nlm.nih.gov/pubmed/19494034
http://dx.doi.org/10.1093/hmg/ddp262

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