Human alpha-synuclein overexpressing MBP29 mice mimic functional and structural hallmarks of the cer...
Human alpha-synuclein overexpressing MBP29 mice mimic functional and structural hallmarks of the cerebellar subtype of multiple system atrophy
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England: BioMed Central Ltd
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English
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England: BioMed Central Ltd
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Multiple system atrophy (MSA) is a rare, but fatal atypical parkinsonian disorder. The prototypical pathological hallmark are oligodendroglial cytoplasmic inclusions (GCIs) containing alpha-synuclein (α-syn). Currently, two MSA phenotypes are classified: the parkinsonian (MSA-P) and the cerebellar subtype (MSA-C), clinically characterized by predom...
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Human alpha-synuclein overexpressing MBP29 mice mimic functional and structural hallmarks of the cerebellar subtype of multiple system atrophy
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TN_cdi_doaj_primary_oai_doaj_org_article_f39eb5bd488a45678683fe0a35439f1a
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_f39eb5bd488a45678683fe0a35439f1a
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ISSN
2051-5960
E-ISSN
2051-5960
DOI
10.1186/s40478-021-01166-x