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dc.contributor.authorPak, Meltem
dc.contributor.authorBilgic, Başar
dc.contributor.authorErginel-Unaltuna, Nihan
dc.contributor.authorGurvit, Hakan
dc.contributor.authorHanagasi, Haşmet Ayhan
dc.contributor.authorKESSLER, Christoph
dc.contributor.authorATASU, Burcu
dc.contributor.authorSIMON-SANCHEZ, Javier
dc.contributor.authorHAUSER, Ann-Kathrin
dc.contributor.authorGASSER, Thomas
dc.contributor.authorLOHMANN, Ebba
dc.date.accessioned2021-03-03T11:53:20Z
dc.date.available2021-03-03T11:53:20Z
dc.identifier.citationKESSLER C., ATASU B., Hanagasi H. A. , SIMON-SANCHEZ J., HAUSER A., Pak M., Bilgic B., Erginel-Unaltuna N., Gurvit H., GASSER T., et al., "Role of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey", PARKINSONISM & RELATED DISORDERS, cilt.48, ss.34-39, 2018
dc.identifier.issn1353-8020
dc.identifier.othervv_1032021
dc.identifier.otherav_2a9a2a85-f493-4bf4-9c95-eb5175f73488
dc.identifier.urihttp://hdl.handle.net/20.500.12627/33415
dc.identifier.urihttps://doi.org/10.1016/j.parkreldis.2017.12.007
dc.description.abstractIntroduction: Mutations in the LRRK2 and alpha-synuclein (SNCA) genes are well-established causes of autosomal dominant Parkinson's disease (PD). However, their frequency differs widely between ethnic groups. Only three studies have screened all coding regions of LRRK2 and SNCA in European samples so far. In Turkey, the role of LRRK2 in Parkinson's disease has been studied fragmentarily, and the incidence of SNCA copy number variations is unknown. The purpose of this study is to determine the frequency of LRRK2 and SNCA mutations in autosomal dominant PD in Turkey.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectNöroloji
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titleRole of LRRK2 and SNCA in autosomal dominant Parkinson's disease in Turkey
dc.typeMakale
dc.relation.journalPARKINSONISM & RELATED DISORDERS
dc.contributor.departmentEberhard Karls University of Tubingen , ,
dc.identifier.volume48
dc.identifier.startpage34
dc.identifier.endpage39
dc.contributor.firstauthorID99152


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