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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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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The American Society for Cell Biology
2006
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| Acesso em linha: | 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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