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dc.contributor.authorHoang, Quyen Q
dc.contributor.authorWang, Wei
dc.contributor.authorPetsko, Gregory A
dc.contributor.authorEmre, Murat
dc.contributor.authorBonifati, Vincenzo
dc.contributor.authorFevga, Christina
dc.contributor.authorPark, Yangshin
dc.contributor.authorLohmann, Ebba
dc.contributor.authorKievit, Anneke J
dc.contributor.authorBreedveld, Guido J
dc.contributor.authorFerraro, Federico
dc.contributor.authorde Boer, Leon
dc.contributor.authorvan Minkelen, Rick
dc.contributor.authorHanagasi, Haşmet Ayhan
dc.contributor.authorBoon, Agnita
dc.date.accessioned2021-12-10T13:15:15Z
dc.date.available2021-12-10T13:15:15Z
dc.identifier.citationFevga C., Park Y., Lohmann E., Kievit A. J. , Breedveld G. J. , Ferraro F., de Boer L., van Minkelen R., Hanagasi H. A. , Boon A., et al., "A new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson's disease.", Parkinsonism & related disorders, cilt.89, ss.63-72, 2021
dc.identifier.issn1353-8020
dc.identifier.othervv_1032021
dc.identifier.otherav_f90bfc95-8a8d-49e2-8daa-c554351111e4
dc.identifier.urihttp://hdl.handle.net/20.500.12627/175747
dc.identifier.urihttps://avesis.istanbul.edu.tr/api/publication/f90bfc95-8a8d-49e2-8daa-c554351111e4/file
dc.identifier.urihttps://doi.org/10.1016/j.parkreldis.2021.06.023
dc.description.abstractIntroduction: Missense variants and multiplications of the alpha-synuclein gene (SNCA) are established as rare causes of autosomal dominant forms of Parkinson's Disease (PD).
dc.language.isoeng
dc.subjectKLİNİK NEUROLOJİ
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.titleA new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson's disease.
dc.typeMakale
dc.relation.journalParkinsonism & related disorders
dc.contributor.department, ,
dc.identifier.volume89
dc.identifier.startpage63
dc.identifier.endpage72
dc.contributor.firstauthorID2741581


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