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Transferrin D Protein Variants in the Diagnosis of Congenital Disorders of Glycosylation (CDG)

Publikace na 1. lékařská fakulta |
2009

Tento text není v aktuálním jazyce dostupný. Zobrazuje se verze "en".Abstrakt

This paper discusses an analytical problem in the differentiation between congenital disorders of glycosylation (CDG; transferrin as a marker of hypoglycosylation) and transferrin protein variants, namely the type D.