Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene

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dc.contributor.author Alber, Michael Wolfgang Hans-Peter de_DE
dc.date.accessioned 2014-04-07T13:03:37Z
dc.date.available 2014-04-07T13:03:37Z
dc.date.issued 2012 de_DE
dc.identifier.issn 0022-2593 de_DE
dc.identifier.uri http://hdl.handle.net/10900/50938
dc.language.iso en en
dc.publisher B M J Publishing Group de_DE
dc.relation.uri http://dx.doi.org/10.1136/jmedgenet-2012-100859 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene de_DE
dc.type Artikel de_DE
utue.quellen.id 20140226071329_02107 de_DE
utue.publikation.seiten 391-399 de_DE
utue.personen.roh Kousi, Maria de_DE
utue.personen.roh Anttila, Verneri de_DE
utue.personen.roh Schulz, Angela de_DE
utue.personen.roh Calafato, Stella de_DE
utue.personen.roh Jakkula, Eveliina de_DE
utue.personen.roh Riesch, Erik de_DE
utue.personen.roh Myllykangas, Liisa de_DE
utue.personen.roh Kalimo, Hannu de_DE
utue.personen.roh Topcu, Meral de_DE
utue.personen.roh Gokben, Sarenur de_DE
utue.personen.roh Alehan, Fusun de_DE
utue.personen.roh Lemke, Johannes R. de_DE
utue.personen.roh Alber, Michael de_DE
utue.personen.roh Palotie, Aarno de_DE
utue.personen.roh Kopra, Outi de_DE
utue.personen.roh Lehesjoki, Anna-Elina de_DE
dcterms.isPartOf.ZSTitelID Journal of Medical Genetics de_DE
dcterms.isPartOf.ZS-Issue 6 de_DE
dcterms.isPartOf.ZS-Volume 49 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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