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Unverricht-Lundborg Disease in Turkey: Delineating The Phenotype Between Cystatin B Mutation Positive and Negative Cases

dc.contributor.authorGunduz, Ayseguel
dc.contributor.authorBebek, Nerses
dc.contributor.authorLehesjoki, Anna-Elina
dc.contributor.authorIlgen-Uslu, Ferda
dc.contributor.authorBaykan, BETÜL
dc.contributor.authorErdinc, Oguz Osman
dc.contributor.authorJoensuu, Tarja
dc.contributor.authorOzkara, Cigdem
dc.contributor.authorTutkavul, Kemal
dc.date.accessioned2021-03-04T15:00:20Z
dc.date.available2021-03-04T15:00:20Z
dc.date.issued2010
dc.identifier.citationErdinc O. O. , Joensuu T., Ilgen-Uslu F., Bebek N., Ozkara C., Tutkavul K., Gunduz 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-TURKISH, cilt.27, sa.1, ss.1-11, 2010
dc.identifier.issn1302-1664
dc.identifier.othervv_1032021
dc.identifier.otherav_847f5b82-b77c-4dea-b973-5f7c587173b4
dc.identifier.urihttp://hdl.handle.net/20.500.12627/90122
dc.description.abstractObjective: We herein report the first three genetically proven Unverricht-Lundborg disease (ULD) patients in Turkey and their clinical comparisons with eight CSTB mutation negative patients who were suspected to have ULD.
dc.language.isoeng
dc.subjectSinirbilim ve Davranış
dc.subjectTemel Bilimler
dc.subjectYaşam Bilimleri
dc.subjectNEUROSCIENCES
dc.subjectYaşam Bilimleri (LIFE)
dc.titleUnverricht-Lundborg Disease in Turkey: Delineating The Phenotype Between Cystatin B Mutation Positive and Negative Cases
dc.typeMakale
dc.relation.journalJOURNAL OF NEUROLOGICAL SCIENCES-TURKISH
dc.contributor.departmentEskişehir Osmangazi Üniversitesi , ,
dc.identifier.volume27
dc.identifier.issue1
dc.identifier.startpage1
dc.identifier.endpage11
dc.contributor.firstauthorID60794


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