Gain-of-function HCN2 variants in genetic epilepsy

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Show simple item record Schubert, Julian Lerche, Holger 2019-12-11T14:25:52Z 2019-12-11T14:25:52Z 2018
dc.identifier.issn 1098-1004
dc.language.iso en en
dc.publisher Wiley de_DE
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title Gain-of-function HCN2 variants in genetic epilepsy de_DE
dc.type Artikel de_DE 20190321153956_03952
utue.publikation.seiten 202-209 de_DE
utue.personen.roh Li, Melody
utue.personen.roh Maljevic, Snezana
utue.personen.roh Phillips, A. Marie
utue.personen.roh Petrovski, Slave
utue.personen.roh Hildebrand, Michael S.
utue.personen.roh Burgess, Rosemary
utue.personen.roh Mount, Therese
utue.personen.roh Zara, Federico
utue.personen.roh Striano, Pasquale
utue.personen.roh Schubert, Julian
utue.personen.roh Thiele, Holger
utue.personen.roh Nuernberg, Peter
utue.personen.roh Wong, Michael
utue.personen.roh Weisenberg, Judith L.
utue.personen.roh Thio, Liu Lin
utue.personen.roh Lerche, Holger
utue.personen.roh Scheffer, Ingrid E.
utue.personen.roh Berkovic, Samuel F.
utue.personen.roh Petrou, Steven
utue.personen.roh Reid, Christopher A.
dcterms.isPartOf.ZSTitelID Human Mutation de_DE
dcterms.isPartOf.ZS-Issue 2 de_DE
dcterms.isPartOf.ZS-Volume 39 de_DE
utue.fakultaet 04 Medizinische Fakultät

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