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Article (Scientific journals)
Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations.
Schmidt, Alexander; Kumar, Kishore R.; Redyk, Katharina et al.
2012 • In Archives of Neurology, 69 (5), p. 668-70
Peer Reviewed verified by ORBi
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https://hdl.handle.net/10993/24254
DOI
10.1001/archneurol.2012.187
PubMed
22782515
 

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Keywords :
Dystonia/genetics; Electroencephalography; Epilepsy, Benign Neonatal/genetics; Family Health; Female; Humans; Male; Membrane Proteins/genetics; Mutation/genetics; Nerve Tissue Proteins/genetics
Disciplines :
UNKNOWN KEY #A01
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 
External co-authors :
yes
Language :
English
Title :
Two faces of the same coin: benign familial infantile seizures and paroxysmal kinesigenic dyskinesia caused by PRRT2 mutations.
Publication date :
2012
Journal title :
Archives of Neurology
ISSN :
0003-9942
eISSN :
1538-3687
Publisher :
American Medical Association, United States - Illinois
Volume :
69
Issue :
5
Pages :
668-70
Peer reviewed :
Peer Reviewed verified by ORBi
Available on ORBilu :
since 05 February 2016

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