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Marrone, L. et al. (2022). SPG15 protein deficits are at the crossroads between lysosomal abnormalities, altered lipid metabolism and synaptic dysfunction. Human molecular genetics. 31 (16), pp. 2693-2710. [Online].
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Marrone, L. et al. (2022). SPG15 protein deficits are at the crossroads between lysosomal abnormalities, altered lipid metabolism and synaptic dysfunction. Human molecular genetics. 31 (16), pp. 2693-2710. [Online].