1. Mitochondrial abnormalities and disruption of the neuromuscular junction precede the clinical phenotype and motor neuron loss in hFUSWT transgenic mice. (28th November 2017) Authors: So, Eva; Mitchell, Jacqueline C; Memmi, Caroline; Chennell, George; Vizcay-Barrena, Gema; Allison, Leanne; Shaw, Christopher E; Vance, Caroline Journal: Human molecular genetics Issue: Volume 27:Number 3(2018:Feb. 01) Page Start: 463 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗