Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia and frontotemporal dementia

Soragia Athina Gkazi, Claire Troakes, Simon Topp, Jack W. Miller, Caroline A. Vance, Jemeen Sreedharan, Ammar Al-Chalabi, Janine Kirby, Pamela J. Shaw, Safa Al-Sarraj, Andrew King, Bradley N. Smith, Christopher E. Shaw

Research output: Contribution to journal › Article › peer-review

14 Citations (Scopus)
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