Phenotypic variability in a dystonia family with mutations in the manganese transporter gene

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Title:	Phenotypic variability in a dystonia family with mutations in the manganese transporter gene
Author(s):	Delnooz, C.C.S. ; Wevers, R.A. ; Quadri, M.; Clayton, P.T.; Mills, P.B.; Tuschl, K.; Steenbergen, E.J.; Bonifati, V.; Warrenburg, B.P.C. van de
Publication year:	2013
Source:	Movement Disorders, vol. 28, iss. 5, (2013), pp. 685-686
ISSN:	0885-3185
DOI:	https://doi.org/10.1002/mds.25390
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/115418
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Subject:	DCN MP - Plasticity and memory DCN MP - Plasticity and memory NCEBP 10: Human Movement & Fatigue DCN NN - Brain networks and neuronal communication DCN PAC - Perception action and control DCN PAC - Perception action and control IGMD 4: Glycostation disorders IGMD 3: Genomic disorders and inherited multi-system disorders Tijdelijke code tbv inlezen publicaties Radboudumc - Alleen voor gebruik door Radboudumc
Organization:	Donders Centre for Cognitive Neuroimaging Neurology Laboratory of Genetic, Endocrine and Metabolic Diseases Paediatrics - OUD tm 2017
Former Organization:	F.C. Donders Centre for Cognitive Neuroimaging
Journal title:	Movement Disorders
Volume:	vol. 28
Issue:	iss. 5
Page start:	p. 685
Page end:	p. 686