Diagnostic serum glycosylation profile in patients with intellectual disability as a result of MAN1B1 deficiency

Author(s):
Scherpenzeel, M. van; Timal, S.; Rymen, D.; Hoischen, A.; Wuhrer, M. (0000-0002-0814-4995); Hipgrave-Ederveen, A.; Grunewald, S.; Peanne, R.; Saada, A.; Edvardson, S.; Gronborg, S.; Ruijter, G.; Kattentidt-Mouravieva, A.; Brum, J.M.; Freckmann, M.L.; Tomkins, S.; Jalan, A.; Prochazkova, D.; Ondruskova, N.; Hansikova, H.; Willemsen, M.A.; Hensbergen, P.J. (0000-0002-3193-5445); Matthijs, G.; Wevers, R.A.; Veltman, J.A.; Morava, E.; Lefeber, D.J.
Published
2014
Publication type
Article / Letter to editor
MAN1B1 (EC 321113)intellectual disabilitycongenital disorders of glycosylationglycomicsbiomarker
Date issued
2014-04-30
Language
English
Is part of
Brain (2014), Vol. 137, p. 1030-1038
hdl
1887/104935
doi
10.1093/brain/awu019