Whole-Exome Sequencing in NF1-Related West Syndrome Leads to the Identification ofKCNC2as a Novel Candidate Gene for Epilepsy

Rademacher, Annika; Schwarz, Niklas; Seiffert, Simone; Pendziwiat, Manuela; Rohr, Axel; van Baalen, Andreas; Helbig, Ingo; Weber, Yvonne; Muhle, Hiltrud

dc.contributor.author	Schwarz, Niklas
dc.contributor.author	Seiffert, Simone
dc.contributor.author	Weber, Yvonne G.
dc.date.accessioned	2021-07-13T09:17:27Z
dc.date.available	2021-07-13T09:17:27Z
dc.date.issued	2020
dc.identifier.issn	1439-1899
dc.identifier.uri	http://hdl.handle.net/10900/117095
dc.language.iso	en	de_DE
dc.publisher	Georg Thieme Verlag KG	de_DE
dc.relation.uri	http://dx.doi.org/10.1055/s-0040-1710524	de_DE
dc.subject.ddc	610	de_DE
dc.title	Whole-Exome Sequencing in NF1-Related West Syndrome Leads to the Identification ofKCNC2as a Novel Candidate Gene for Epilepsy	de_DE
dc.type	Article	de_DE
utue.quellen.id	20210304112512_01376
utue.publikation.seiten	368-372	de_DE
utue.personen.roh	Rademacher, Annika
utue.personen.roh	Schwarz, Niklas
utue.personen.roh	Seiffert, Simone
utue.personen.roh	Pendziwiat, Manuela
utue.personen.roh	Rohr, Axel
utue.personen.roh	van Baalen, Andreas
utue.personen.roh	Helbig, Ingo
utue.personen.roh	Weber, Yvonne
utue.personen.roh	Muhle, Hiltrud
dcterms.isPartOf.ZSTitelID	Neuropediatrics	de_DE
dcterms.isPartOf.ZS-Issue	5	de_DE
dcterms.isPartOf.ZS-Volume	51	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE