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Unverricht-Lundborg disease in Turkey: Delineating the phenotype between cystatin B mutation positive and negative cases

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dc.contributor.authorErdinç, Oǧuz Osman
dc.contributor.authorJoensuu, Tarja
dc.contributor.authorBEBEK, Nerses
dc.contributor.authorÖzkara, Çiǧdem
dc.contributor.authorTutkavul, Kemal
dc.contributor.authorGündüz, Ayşegül
dc.contributor.authorLehesjoki, Anna-Elina
dc.contributor.authorBaykan, Betül
dc.contributor.institutionauthorUSLU, FERDA
dc.date.accessioned2019-12-31T20:59:18Z
dc.date.available2019-12-31T20:59:18Z
dc.date.issued2010-04-16
dc.identifier.citationErdinç O. O. , Joensuu T., Ilǧen-Uslu F., BEBEK N., Özkara Ç., Tutkavul K., Gündüz A., Lehesjoki A., Baykan B., -Unverricht-Lundborg disease in Turkey: Delineating the phenotype between cystatin B mutation positive and negative cases-, Journal of Neurological Sciences, cilt.27, ss.1-11, 2010
dc.identifier.urihttps://hdl.handle.net/20.500.12645/11146
dc.titleUnverricht-Lundborg disease in Turkey: Delineating the phenotype between cystatin B mutation positive and negative cases
dc.typeArticle
dspace.entity.typePublication
local.avesis.id847f5b82-b77c-4dea-b973-5f7c587173b4
relation.isAuthorOfPublicationd406911e-cc19-4fcf-93a8-cff8677e582a
relation.isAuthorOfPublication.latestForDiscoveryd406911e-cc19-4fcf-93a8-cff8677e582a
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