Original paper
"Frontotemporoparietal" dementia: Clinical phenotype associated with the c.709-1G>A PGRN mutation
Abstract
Mutations in the progranulin gene (PGRN) are a major cause of frontotemporal lobar degeneration with tau-negative and ubiquitin-positive neuronal inclusions. Most previous studies aimed at characterizing the clinical and neuropsychological phenotype of PGRN mutation carriers included patients with different PGRN mutations, assuming that the common proposed pathogenetic mechanism of haploinsufficiency will lead to a comparable phenotype.We...
Paper Details
Title
"Frontotemporoparietal" dementia: Clinical phenotype associated with the c.709-1G>A PGRN mutation
Published Date
Oct 27, 2009
Journal
Volume
73
Issue
17
Pages
1367 - 1374
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Notes
History