Publication:
A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood

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dc.contributor.authorYILDIZ, Edibe Pembegul
dc.contributor.authorYEŞİL, GÖZDE
dc.contributor.authorOZKAN, Melis Ulak
dc.contributor.authorBEKTAS, Gonca
dc.contributor.authorCALISKAN, Mine
dc.contributor.authorOZMEN, Meral
dc.contributor.institutionauthorYEŞİL, GÖZDE
dc.date.accessioned2019-10-05T14:16:47Z
dc.date.available2019-10-05T14:16:47Z
dc.date.issued2017-10-01
dc.identifier10.1016/j.arr.2019.02.003
dc.identifier.citationYILDIZ E. P. , YEŞİL G., OZKAN M. U. , BEKTAS G., CALISKAN M., OZMEN M., -A novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood-, Seizure, cilt.51, ss.77-79, 2017
dc.identifier.pubmed28818698
dc.identifier.urihttps://hdl.handle.net/20.500.12645/3437
dc.language.isoen
dc.titleA novel EPM2A mutation in a patient with Lafora disease presenting with early parkinsonism symptoms in childhood
dc.typeArticle
dspace.entity.typePublication
local.article.journalnameAgeing research reviews
local.avesis.id5399e2da-0b10-41a8-95c6-18339e956415
local.avesis.response3307
relation.isAuthorOfPublicationb653abbc-327a-4b3b-a227-f3344d8d6b70
relation.isAuthorOfPublication.latestForDiscoveryb653abbc-327a-4b3b-a227-f3344d8d6b70
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