@article{article, title = {{Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia}}, url = {{http://eprints.whiterose.ac.uk/139464/ }}, year = {{2019}}, month = {{1}}, author = {{Gkazi SA and Troakes C and Topp S and Miller JW and Vance CA and Sreedharan J and Al-Chalabi A and Kirby J and Shaw PJ and Al-Sarraj S and King A et al}}, doi = {{10.1016/j.neurobiolaging.2018.08.015}}, volume = {{73}}, journal = {{Neurobiology of Aging}}, pages = {{229.e5-229.e9}}, note = {{Accessed on 2025/03/13}}}