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Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia
scholarly article by Soragia Athina Gkazi et al published 24 August 2018 in Neurobiology of Aging
Author/s
author: Ammar Al-Chalabi, Claire Troakes, Soragia Athina Gkazi, Jemeen Sreedharan, Simon Topp, Bradley N. Smith, Caroline Vance
Work details
Publication date
August 24, 2018
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Language
English
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