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N-glycome analysis detects dysglycosylation missed by conve..:
Park, Julien H
;
Mealer, Robert G
;
Elias, Abdallah F
...
Journal of Inherited Metabolic Disease, 0141-8955, 2020, 43:6, s. 1370-1381. , 2020
Link:
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-17581
RT Journal T1
N-glycome analysis detects dysglycosylation missed by conventional methods in SLC39A8 deficiency
UL https://suche.suub.uni-bremen.de/peid=base-ftumeauniv:oai:DiVA.org:umu-175818&Exemplar=1&LAN=DE A1 Park, Julien H A1 Mealer, Robert G A1 Elias, Abdallah F A1 Hoffmann, Susanne A1 Grueneberg, Marianne A1 Biskup, Saskia A1 Fobker, Manfred A1 Haven, Jaclyn A1 Mangels, Ute A1 Reunert, Janine A1 Rust, Stephan A1 Schoof, Jonathan A1 Schwanke, Corbin A1 Smoller, Jordan W A1 Cummings, Richard D A1 Marquardt, Thorsten PB Umeå universitet, Neurovetenskaper; Department of General Pediatrics, University of Münster, Münster, Germany YR 2020 K1 congenital disorders of glycosylation K1 glycosylation K1 MALDI-TOF MS K1 manganese K1 Cell and Molecular Biology K1 Cell- och molekylärbiologi JF Journal of Inherited Metabolic Disease, 0141-8955, 2020, 43:6, s. 1370-1381 LK http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-175818 DO http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-175818 SF ELIB - SuUB Bremen
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