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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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| Hlavní autoři: | , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2009
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| Témata: | |
| On-line přístup: | 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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