Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulation.

Reference : Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain ...


	Document type :	Scientific journals : Article
	Discipline(s) :	Life sciences : Genetics & genetic processes
	To cite this reference:	http://hdl.handle.net/10993/17159

Title :	Novel ATP1A3 mutation in a sporadic RDP patient with minimal benefit from deep brain stimulation.
Language :	English
Author, co-author :	Kamm, C. [> >]
	Fogel, W. [> >]
	Wachter, T. [> >]
	Schweitzer, K. [> >]
	Berg, D. [> >]
	Krüger, Rejko [University of Luxembourg > Faculty of Science, Technology and Communication (FSTC) > Life Science Research Unit]
	Freudenstein, D. [> >]
	Gasser, T. [> >]
Publication date :	2008
Journal title :	Neurology
Volume :	70
Issue/season :	16 Pt 2
Pages :	1501-3
Peer reviewed :	Yes (verified by ORBi^lu)
ISSN :	0028-3878
e-ISSN :	1526-632X
Country :	United States
Keywords :	[en] Adult ; Age of Onset ; Deep Brain Stimulation/methods ; Dystonia/complications/genetics/therapy ; Humans ; Male ; Mutation/genetics ; Parkinsonian Disorders/complications/genetics/therapy ; Sodium-Potassium-Exchanging ATPase/genetics
Permalink :	http://hdl.handle.net/10993/17159

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