Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.

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Title:	Severe episodic neurological deficits and permanent mental retardation in a child with a novel FHM2 ATP1A2 mutation.
Author(s):	Vanmolkot, K.R.; Stroink, H.; Koenderink, J.B. ; Kors, E.E.; Heuvel, J.J.M.W. van den ; Boogerd, E.H. van den; Stam, A.H.; Haan, J.H.A. de; Vries, B. de ; Terwindt, G.M.
Publication year:	2006
Source:	Annals of Neurology, vol. 59, iss. 2, (2006), pp. 310-314
ISSN:	0364-5134
DOI:	https://doi.org/10.1002/ana.20760
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : http://hdl.handle.net/2066/49308
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Subject:	DCN 2: Functional Neurogenomics IGMD 3: Genomic disorders and inherited multi-system disorders N4i 1: Pathogenesis and modulation of inflammation N4i 3: Poverty-related infectious diseases NCMLS 5: Membrane transport and intracellular motility UMCN 5.1: Genetic defects of metabolism UMCN 5.4: Renal disorders
Organization:	Pharmacology-Toxicology Radiology Human Genetics
Former Organization:	Pharmacology/Toxicology
Journal title:	Annals of Neurology
Volume:	vol. 59
Issue:	iss. 2
Page start:	p. 310
Page end:	p. 314

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