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Mitochondrial dysfunction in hereditary spastic paraparesis with mutations in DDHD1/SPG28.
scientific article published on 4 February 2016
Author/s
author: Anna Rubegni, Stefano Doccini, Filippo Maria Santorelli, Alessandra Tessa, Maria Teresa Dotti, Alessandro Malandrini, Andrea Mignarri, Maria Chiara Meschini, Elena Cardaioli
Work details
Publication date
February 4, 2016
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Language
English
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