@article{article, title  = {{Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia}},

 publisher = {{Elsevier}},

 url = {{https://eprints.whiterose.ac.uk/id/eprint/139464 https://doi.org/10.1016/j.neurobiolaging.2018.08.015 }},

 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 2025/11/01}}}