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[Despite a plethora of modifications demonstrated for different neurodegeneration-related proteins, such as amyloid-?, prion protein, tau, ?-synuclein, TAR DNA-binding protein 43 (TDP-43), or fused in sarcoma protein (FUS), molecular classification of NDDs relies on detailed morphological evaluation of protein deposits, their distribution in the brain, and their correlation to clinical symptoms together with specific genetic alterations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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