TY - JOUR
T1 - Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia
JO - Neurobiology of Aging
UR - http://eprints.whiterose.ac.uk/139464/
PY - 2019/01/01
AU - Gkazi SA
AU - Troakes C
AU - Topp S
AU - Miller JW
AU - Vance CA
AU - Sreedharan J
AU - Al-Chalabi A
AU - Kirby J
AU - Shaw PJ
AU - Al-Sarraj S
AU - King A et al
ED -
DO - DOI: 10.1016/j.neurobiolaging.2018.08.015
VL - 73
SP - 229.e5
EP - 229.e9
Y2 - 2025/07/04
ER -