Striking Phenotypic Variation in a Family With the P506S UBQLN2 Mutation Including Amyotrophic Lateral Sclerosis, Spastic Paraplegia and Frontotemporal Dementia
Neurobiology of Aging - United States
doi 10.1016/j.neurobiolaging.2018.08.015
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Date
January 1, 2019
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Elsevier BV