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Sabina Capellari
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Characterization of the F198S prion protein mutation: enhanced glycosylation and defective refolding.
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scientific article
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study
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scholarly article by Marialuisa Quadri et al published July 2018 in Lancet Neurology