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A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion

dc.contributor.authorSevim, S
dc.contributor.authorApaydin, Hülya
dc.contributor.authorOzekmekci, S
dc.contributor.authorGwinn-Hardy, K
dc.contributor.authorSingleton, A
dc.contributor.authorDogu, O
dc.contributor.authorJohnson, J
dc.contributor.authorHernandez, D
dc.contributor.authorHanson, M
dc.contributor.authorHardy, J
dc.date.accessioned2021-03-05T08:24:51Z
dc.date.available2021-03-05T08:24:51Z
dc.date.issued2004
dc.identifier.citationDogu O., Johnson J., Hernandez D., Hanson M., Hardy J., Apaydin H., Ozekmekci S., Sevim S., Gwinn-Hardy K., Singleton A., "A consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion", MOVEMENT DISORDERS, cilt.19, ss.812-816, 2004
dc.identifier.issn0885-3185
dc.identifier.otherav_98bf7b93-6202-4930-8e03-0ff90086f2fe
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/102770
dc.identifier.urihttps://doi.org/10.1002/mds.20028
dc.description.abstractThe importance of parkin in early-onset Parkinson's disease in Japan, Europe, and the United States is well established. The contribution of this gene to the risk of Parkinson's disease in other populations is less well known. To explore the importance of parkin in those of Turkish ancestry, we studied familial cases from that country, and identified a consanguineous family with early-onset Parkinson's disease due to a homozygous mutation in parkin. (C) 2004 Movement Disorder Society.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleA consanguineous Turkish family with early-onset Parkinson's disease and an exon 4 parkin deletion
dc.typeMakale
dc.relation.journalMOVEMENT DISORDERS
dc.contributor.department, ,
dc.identifier.volume19
dc.identifier.issue7
dc.identifier.startpage812
dc.identifier.endpage816
dc.contributor.firstauthorID21997


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