Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene

Kousi, Maria; Anttila, Verneri; Schulz, Angela; Calafato, Stella; Jakkula, Eveliina; Riesch, Erik; Myllykangas, Liisa; Kalimo, Hannu; Topcu, Meral; Gokben, Sarenur; Alehan, Fusun; Lemke, Johannes R.; Alber, Michael; Palotie, Aarno; Kopra, Outi; Lehesjoki, Anna-Elina

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	Article	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