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COG-7-deficient Human Fibroblasts Exhibit Altered Recycling of Golgi Proteins

Recently, we reported that two siblings presenting with the clinical syndrome congenital disorders of glycosylation (CDG) have mutations in the gene encoding Cog7p, a member of the conserved oligomeric Golgi (COG) complex. In this study, we analyzed the localization and trafficking of multiple Golgi...

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Autors principals: Steet, Richard, Kornfeld, Stuart
Format: Artigo
Idioma:Inglês
Publicat: The American Society for Cell Biology 2006
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1446086/
https://ncbi.nlm.nih.gov/pubmed/16510524
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E05-08-0822
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