GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers

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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 Artikel 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


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