dc.contributor.author |
Hedrich, Ulrike B. S. |
|
dc.contributor.author |
Elsen, Gina |
|
dc.date.accessioned |
2018-10-23T08:55:57Z |
|
dc.date.available |
2018-10-23T08:55:57Z |
|
dc.date.issued |
2016 |
|
dc.identifier.issn |
1537-6605 |
|
dc.identifier.uri |
http://hdl.handle.net/10900/84464 |
|
dc.language.iso |
en |
de_DE |
dc.publisher |
Cell Press |
de_DE |
dc.relation.uri |
http://dx.doi.org/10.1016/j.ajhg.2016.07.013 |
de_DE |
dc.rights |
info:eu-repo/semantics/closedAccess |
|
dc.subject.ddc |
570 |
de_DE |
dc.subject.ddc |
610 |
de_DE |
dc.title |
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers |
de_DE |
dc.type |
Article |
de_DE |
utue.quellen.id |
20180405102126_00739 |
|
utue.publikation.seiten |
802-816 |
de_DE |
utue.personen.roh |
Li, Dong |
|
utue.personen.roh |
Yuan, Hongjie |
|
utue.personen.roh |
Ortiz-Gonzalez, Xilma R. |
|
utue.personen.roh |
Marsh, Eric D. |
|
utue.personen.roh |
Tian, Lifeng |
|
utue.personen.roh |
McCormick, Elizabeth M. |
|
utue.personen.roh |
Kosobucki, Gabrielle J. |
|
utue.personen.roh |
Chen, Wenjuan |
|
utue.personen.roh |
Schulien, Anthony J. |
|
utue.personen.roh |
Chiavacci, Rosetta |
|
utue.personen.roh |
Tankovic, Anel |
|
utue.personen.roh |
Naase, Claudia |
|
utue.personen.roh |
Brueckner, Frieder |
|
utue.personen.roh |
Hu, Chun |
|
utue.personen.roh |
Kusumoto, Hirofumi |
|
utue.personen.roh |
Hedrich, Ulrike B. S. |
|
utue.personen.roh |
Elsen, Gina |
|
utue.personen.roh |
Aizenman, Elias |
|
utue.personen.roh |
Lemke, Johannes R. |
|
utue.personen.roh |
Hakonarson, Hakon |
|
utue.personen.roh |
Traynelis, Stephen F. |
|
utue.personen.roh |
Falk, Marni J. |
|
utue.personen.roh |
von Stülpnagel-Steinbeis, Celina |
|
utue.personen.roh |
Hörtnagel, Konstanze |
|
dcterms.isPartOf.ZSTitelID |
American Journal of Human Genetics |
de_DE |
dcterms.isPartOf.ZS-Issue |
4 |
de_DE |
dcterms.isPartOf.ZS-Volume |
99 |
de_DE |
utue.fakultaet |
04 Medizinische Fakultät |
de_DE |