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

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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 Artikel 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


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