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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Detalles Bibliográficos
Autores principales: Bruggink, Cees, Poorthuis, Ben J. H. M., Deelder, André M., Wuhrer, Manfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354319/
https://www.ncbi.nlm.nih.gov/pubmed/22526647
http://dx.doi.org/10.1007/s00216-012-5968-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3354319/
https://www.ncbi.nlm.nih.gov/pubmed/22526647
http://dx.doi.org/10.1007/s00216-012-5968-9

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