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Vincenzo Bonifati
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4
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study
scholarly article by Marialuisa Quadri et al published July 2018 in Lancet Neurology
Manganese transport disorder: Novel SLC30A10 mutations and early phenotypes
scientific article published on March 17, 2015
Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease
scientific article published on February 16, 2012
Analysis of LRRK2, SNCA, Parkin, PINK1, and DJ-1 in Zambian patients with Parkinson's disease
scientific article published on March 24, 2012
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