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

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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


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