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Transferrin D protein variants in the diagnosis of congenital disorders of glycosylation (CDG)
Congenital disorders of glycosylation are a rapidly growing group of inherited (neuro)metabolic disorders characterized by defects in glycosylation of proteins and lipids. This study discusses an analytical problem in the differentiation between hypoglycosylation and transferrin (Tf) protein variant...
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| Pubblicato in: | J Clin Lab Anal |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Wiley Subscription Services, Inc., A Wiley Company
2009
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6648993/ https://ncbi.nlm.nih.gov/pubmed/19288450 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.20293 |
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