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    So, E., Mitchell, J. C., Memmi, C., Chennell, G., Vizcay-Barrena, G., Allison, L., Shaw, C. E., & Vance, C. (n.d.). mitochondrial abnormalities and disruption of the neuromuscular junction precede the clinical phenotype and motor neuron loss in hFUSWT transgenic mice. Human molecular genetics, 27, 463–474. http://access.bl.uk/ark:/81055/vdc_100095495468.0x000031