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  - 2024/12/25

ER  -