dc.contributor.author |
Weber, Yvonne G. |
de_DE |
dc.contributor.author |
Lerche, Holger |
de_DE |
dc.contributor.author |
Becker, Felicitas |
de_DE |
dc.contributor.author |
Ried, Janina S. |
de_DE |
dc.date.accessioned |
2013-07-17T13:13:17Z |
|
dc.date.available |
2013-07-17T13:13:17Z |
|
dc.date.issued |
2013 |
de_DE |
dc.identifier.issn |
0013-9580 |
de_DE |
dc.identifier.uri |
http://hdl.handle.net/10900/36033 |
|
dc.language.iso |
en |
en |
dc.publisher |
Wiley - Blackwell |
de_DE |
dc.relation.uri |
http://dx.doi.org/10.1111/epi.12084 |
de_DE |
dc.rights |
info:eu-repo/semantics/closedAccess |
|
dc.subject.ddc |
610 |
de_DE |
dc.title |
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy |
de_DE |
dc.type |
Article |
de_DE |
utue.quellen.id |
20130315161744_00085 |
de_DE |
utue.publikation.seiten |
265-271 |
de_DE |
utue.personen.roh |
Lal, Dennis |
de_DE |
utue.personen.roh |
Trucks, Holger |
de_DE |
utue.personen.roh |
Moller, Rikke S. |
de_DE |
utue.personen.roh |
Hjalgrim, Helle |
de_DE |
utue.personen.roh |
Koeleman, Bobby P. C. |
de_DE |
utue.personen.roh |
de Kovel, Carolien G. F. |
de_DE |
utue.personen.roh |
Visscher, Frank |
de_DE |
utue.personen.roh |
Weber, Yvonne G. |
de_DE |
utue.personen.roh |
Lerche, Holger |
de_DE |
utue.personen.roh |
Becker, Felicitas |
de_DE |
utue.personen.roh |
Schankin, Christoph J. |
de_DE |
utue.personen.roh |
Neubauer, Bernd A. |
de_DE |
utue.personen.roh |
Surges, Rainer |
de_DE |
utue.personen.roh |
Kunz, Wolfram S. |
de_DE |
utue.personen.roh |
Zimprich, Fritz |
de_DE |
utue.personen.roh |
Franke, Andre |
de_DE |
utue.personen.roh |
Illig, Thomas |
de_DE |
utue.personen.roh |
Ried, Janina S. |
de_DE |
utue.personen.roh |
Leu, Costin |
de_DE |
utue.personen.roh |
Nuernberg, Peter |
de_DE |
utue.personen.roh |
Sander, Thomas |
de_DE |
dcterms.isPartOf.ZSTitelID |
Epilepsia |
de_DE |
dcterms.isPartOf.ZS-Issue |
2 |
de_DE |
dcterms.isPartOf.ZS-Volume |
54 |
de_DE |
utue.fakultaet |
04 Medizinische Fakultät |
de_DE |