Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations
Abstract
Background: Frontotemporal lobar degeneration (FTLD) is a progressive dementia characterized by focal atrophy of frontal and/or temporal lobes caused by mutations in the gene coding for sequestosome 1 (SQSTM1), among other genes. Rare SQSTM1 gene mutations have been associated with Paget’s disease of bone, amyotrophic lateral sclerosis, and, more recently, frontotemporal lobar degeneration (FTLD). Objective: The aim of the study was to determine...
Paper Details
Title
Neuroimaging Correlates of Frontotemporal Dementia Associated with SQSTM1 Mutations
Published Date
Jun 22, 2016
Volume
53
Issue
1
Pages
303 - 313
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