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Multiple system atrophy (MSA) is a neurodegenerativedisorder characterized by glial cytoplasmic inclusions(GCIs)1composed ofα-synuclein aggregates as neuropatho-logical hallmarks.2In vivo visualization ofα-synucleinpathologies potentially offers diagnostic assessments ofMSA, but has been challenging because of the lack of sensi-tive imaging agents.
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Matsuoka et al. (2022) studied this question.
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