Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11.

Ann Clin Transl Neurol · 2014 · PMC4078876 · PMID 24999486

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a nonsignificant trendno p-value reported

Lysosomal enzyme activities appeared normal across all SPG15 and SPG11 cell lines tested, though there was a nonsignificant trend toward slightly decreased activity (Fig. 7 ).

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