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Genetic variants of transferrin in the diagnosis of protein hypoglycosylation

✍ Scribed by Z. Albahri; E. Marklová; H. Vaníček; L. Minxová; P. Dédek; S. Skálová

Publisher
Springer
Year
2005
Tongue
English
Weight
128 KB
Volume
28
Category
Article
ISSN
0141-8955

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## Abstract 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) pr