Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations.

Reference : Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesig...


	Document type :	Scientific journals : Article
	Discipline(s) :	Scientific journals : Article
	To cite this reference:	http://hdl.handle.net/10993/24254

Title :	Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations.
Language :	English
Author, co-author :	Schmidt, Alexander [> >]
	Kumar, Kishore R. [> >]
	Redyk, Katharina [> >]
	Grünewald, Anne [> >]
	Leben, Matthias [> >]
	Munchau, Alexander [> >]
	Sue, Carolyn M. [> >]
	Hagenah, Johann [> >]
	Hartmann, Hans [> >]
	Lohmann, Katja [> >]
	Christen, Hans-Jurgen [> >]
	Klein, Christine [> >]
Publication date :	2012
Journal title :	Archives of neurology
Volume :	69
Issue/season :	5
Pages :	668-70
Peer reviewed :	Yes (verified by ORBi^lu)
ISSN :	0003-9942
e-ISSN :	1538-3687
Country :	United States
Keywords :	[en] Dystonia/genetics ; Electroencephalography ; Epilepsy, Benign Neonatal/genetics ; Family Health ; Female ; Humans ; Male ; Membrane Proteins/genetics ; Mutation/genetics ; Nerve Tissue Proteins/genetics
Permalink :	http://hdl.handle.net/10993/24254
DOI :	10.1001/archneurol.2012.187

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