Abnormal cartilage development and altered N-glycosylation in Tmem165-deficient zebrafish mirrors the phenotypes associated with TMEM165-CDG

The congenital disorders of glycosylation (CDG), a group of inherited diseases characterized by aberrant glycosylation, encompass a wide range of defects, including glycosyltransferases, glycosidases, nucleotide-sugar transporters as well as proteins involved in maintaining Golgi architecture, pH an...

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Опубликовано в: :Glycobiology
Главные авторы: Bammens, Riet, Mehta, Nickita, Race, Valérie, Foulquier, François, Jaeken, Jaak, Tiemeyer, Michael, Steet, Richard, Matthijs, Gert, Flanagan-Steet, Heather
Формат: Artigo
Язык:Inglês
Опубликовано: Oxford University Press 2015
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Original Articles
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4410832/
https://ncbi.nlm.nih.gov/pubmed/25609749
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/glycob/cwv009
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