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Mutations in STT3A and STT3B cause two congenital disorders of glycosylation
We describe two unreported types of congenital disorders of glycosylation (CDG) which are caused by mutations in different isoforms of the catalytic subunit of the oligosaccharyltransferase (OST). Each isoform is encoded by a different gene (STT3A or STT3B), resides in a different OST complex and ha...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3888133/ https://ncbi.nlm.nih.gov/pubmed/23842455 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt312 |
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