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