A case of fatal Type I congenital disorders of glycosylation (CDG I) associated with low dehydrodolichol diphosphate synthase (DHDDS) activity

BACKGROUND: Type I congenital disorders of glycosylation (CDG-I) are mostly complex multisystemic diseases associated with hypoglycosylated serum glycoproteins. A subgroup harbour mutations in genes necessary for the biosynthesis of the dolichol-linked oligosaccharide (DLO) precursor that is essenti...

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Detalles Bibliográficos
Autores principales: Sabry, S., Vuillaumier-Barrot, S., Mintet, E., Fasseu, M., Valayannopoulos, V., Héron, D., Dorison, N., Mignot, C., Seta, N., Chantret, I., Dupré, T., Moore, S. E. H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919849/
https://www.ncbi.nlm.nih.gov/pubmed/27343064
http://dx.doi.org/10.1186/s13023-016-0468-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919849/
https://www.ncbi.nlm.nih.gov/pubmed/27343064
http://dx.doi.org/10.1186/s13023-016-0468-1

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