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Serum transferrin carrying the xeno-tetrasaccharide NeuAc-Gal-GlcNAc(2) is a biomarker of ALG1-CDG
ALG1-CDG (formerly CDG-Ik) is a subtype of congenital disorders of glycosylation (CDG) where the genetic defect disrupts the synthesis of the lipid-linked oligosaccharide precursor required for N-glycosylation. The initial step in the investigation for these disorders involves the demonstration of h...
Tallennettuna:
| Julkaisussa: | J Inherit Metab Dis |
|---|---|
| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4822552/ https://ncbi.nlm.nih.gov/pubmed/26335155 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-015-9884-y |
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