Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia
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| Description | scholarly article by Soragia Athina Gkazi et al published 24 August 2018 in Neurobiology of Aging |
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| Publication date | August 24, 2018 |
| Language | English |
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