Analysis of urinary oligosaccharides in lysosomal storage disorders by capillary high-performance anion-exchange chromatography–mass spectrometry

Many lysosomal storage diseases are characterized by an increased urinary excretion of glycoconjugates and oligosaccharides that are characteristic for the underlying enzymatic defect. Here, we have used capillary high-performance anion-exchange chromatography (HPAEC) hyphenated to mass spectrometry...

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Bibliografiske detaljer
Main Authors: Bruggink, Cees, Poorthuis, Ben J. H. M., Deelder, André M., Wuhrer, Manfred
Format: Artigo
Sprog:Inglês
Udgivet: Springer-Verlag 2012
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Original Paper
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3354319/
https://ncbi.nlm.nih.gov/pubmed/22526647
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00216-012-5968-9
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