α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism

dc.creator	Sokratous M., Breza M., Senkevich K., Gan-Or Z., Kalampokini S., Spanaki C., Provatas A., Zaunmuktane Z., Valotassiou V., Georgoulias P., Efthymiou S., Hadjigeorgiou G.M., Houlden H., Xiromerisiou G.	en
dc.date.accessioned	2023-01-31T09:58:40Z
dc.date.available	2023-01-31T09:58:40Z
dc.date.issued	2021
dc.identifier	10.1002/mds.28735
dc.identifier.issn	08853185
dc.identifier.uri	http://hdl.handle.net/11615/79169
dc.description.abstract	[No abstract available]	en
dc.language.iso	en	en
dc.source	Movement Disorders	en
dc.source.uri	https://www.scopus.com/inward/record.uri?eid=2-s2.0-85115138092&doi=10.1002%2fmds.28735&partnerID=40&md5=2279aaa879b9726ad79366d6b8ea9339
dc.subject	alpha synuclein	en
dc.subject	alpha synuclein	en
dc.subject	SNCA protein, human	en
dc.subject	gene mutation	en
dc.subject	human	en
dc.subject	Letter	en
dc.subject	parkinsonism	en
dc.subject	phenotype	en
dc.subject	diagnostic imaging	en
dc.subject	genetics	en
dc.subject	mutation	en
dc.subject	phenotype	en
dc.subject	alpha-Synuclein	en
dc.subject	Humans	en
dc.subject	Mutation	en
dc.subject	Parkinsonian Disorders	en
dc.subject	Phenotype	en
dc.subject	John Wiley and Sons Inc	en
dc.title	α-Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism	en
dc.type	other	en

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