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PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism

dc.contributor.authorGurvit, Hakan
dc.contributor.authorBilgic, Basar
dc.contributor.authorErginul-Unaltuna, Nihan
dc.contributor.authorHanagasi, Haşmet Ayhan
dc.contributor.authorGuven, Gamze
dc.contributor.authorGiri, Anamika
dc.contributor.authorHauser, Ann-Kathrin
dc.contributor.authorHeutink, Peter
dc.contributor.authorGasser, Thomas
dc.contributor.authorLohmann, Ebba
dc.contributor.authorSimon-Sanchez, Javier
dc.date.accessioned2021-03-03T10:25:07Z
dc.date.available2021-03-03T10:25:07Z
dc.identifier.citationGiri A., Guven G., Hanagasi H. A. , Hauser A., Erginul-Unaltuna N., Bilgic B., Gurvit H., Heutink P., Gasser T., Lohmann E., et al., "PLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism", TREMOR AND OTHER HYPERKINETIC MOVEMENTS, cilt.6, 2016
dc.identifier.othervv_1032021
dc.identifier.otherav_226235ad-4b43-4b9c-aeed-5f30435b87af
dc.identifier.urihttp://hdl.handle.net/20.500.12627/28146
dc.identifier.urihttps://doi.org/10.7916/d81g0m12
dc.description.abstractBackground: PLA2G6-associated neurodegeneration (PLAN) is a recessive neurodegenerative disorder characterized by three distinct phenotypes: infantile neuroaxonal dystrophy (INAD), atypical neuroaxonal dystrophy (atypical NAD), and PLA2G6-related dystonia-parkinsonism.
dc.language.isoeng
dc.subjectNöroloji
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKLİNİK NEUROLOJİ
dc.titlePLA2G6 Mutations Related to Distinct Phenotypes: A New Case with Early-onset Parkinsonism
dc.typeMakale
dc.relation.journalTREMOR AND OTHER HYPERKINETIC MOVEMENTS
dc.contributor.departmentEberhard Karls University of Tubingen , ,
dc.identifier.volume6
dc.contributor.firstauthorID228750


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