A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression

Buerk, Katrin; Kaiser, Frank J.; Tennstedt, Stephanie; Schoels, Ludger; Kreuz, Friedmar R.; Wieland, Thomas; Stromf, Tim M.; Buettner, Thomas; Hollstein, Ronja; Braunholz, Diana; Plaschke, Jens; Gillessen-Kaesbach, Gabriele; Zuehlke, Christine

dc.contributor.author	Schöls, Ludger
dc.contributor.author	Strom, Tim M.
dc.date.accessioned	2014-08-05T13:39:06Z
dc.date.available	2014-08-05T13:39:06Z
dc.date.issued	2014
dc.identifier.issn	1769-7212
dc.identifier.uri	http://hdl.handle.net/10900/55198
dc.language.iso	en	de_DE
dc.publisher	Elsevier Science Bv	de_DE
dc.relation.uri	http://dx.doi.org/10.1016/j.ejmg.2014.01.005	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression	de_DE
dc.type	Article	de_DE
utue.quellen.id	20140610213910_00182	de_DE
utue.publikation.seiten	207-211	de_DE
utue.personen.roh	Buerk, Katrin
utue.personen.roh	Kaiser, Frank J.
utue.personen.roh	Tennstedt, Stephanie
utue.personen.roh	Schoels, Ludger
utue.personen.roh	Kreuz, Friedmar R.
utue.personen.roh	Wieland, Thomas
utue.personen.roh	Stromf, Tim M.
utue.personen.roh	Buettner, Thomas
utue.personen.roh	Hollstein, Ronja
utue.personen.roh	Braunholz, Diana
utue.personen.roh	Plaschke, Jens
utue.personen.roh	Gillessen-Kaesbach, Gabriele
utue.personen.roh	Zuehlke, Christine
dcterms.isPartOf.ZSTitelID	European Journal of Medical Genetics	de_DE
dcterms.isPartOf.ZS-Issue	5	de_DE
dcterms.isPartOf.ZS-Volume	57	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE