An Unexplained Congenital Disorder of Glycosylation-II in a Child with Neurohepatic Involvement, Hypercholesterolemia and Hypoceruloplasminemia

There is no fulltext present in this item.

Title:	An Unexplained Congenital Disorder of Glycosylation-II in a Child with Neurohepatic Involvement, Hypercholesterolemia and Hypoceruloplasminemia
Author(s):	Calvo, P.L.; Spada, M.; Rabbone, I.; Pinon, M.; Porta, F.; Cisarò, F.; Reggiani, S.; Cefalù, A.B.; Sturiale, L.; Garozzo, D.; Lefeber, D.J. ; Jaeken, J.
Publication year:	2018
Source:	Jimd Reports, vol. 38, (2018), pp. 97-100
ISSN:	2192-8304
DOI:	https://doi.org/10.1007/8904_2017_35
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/190999
Display more details
Subject:	Radboudumc 3: Disorders of movement DCMN: Donders Center for Medical Neuroscience
Organization:	Neurology Laboratory Medicine
Journal title:	Jimd Reports
Volume:	vol. 38
Page start:	p. 97
Page end:	p. 100