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Publications by Simon Topp

Striking Phenotypic Variation in a Family With the P506S UBQLN2 Mutation Including Amyotrophic Lateral Sclerosis, Spastic Paraplegia and Frontotemporal Dementia

Neurobiology of Aging
AgingGerontologyDevelopmental BiologyGeriatricsNeuroscienceNeurology
2019English

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