Open AccessParietal Lobe Deficits in Frontotemporal Lobar Degeneration Caused by a Mutation in the Progranulin Gene
Author(s) -
Jonathan D. Rohrer,
Jason D. Warren,
Rohani Omar,
Simon Mead,
Jonathan Beck,
Tamás Révész,
Janice L. Holton,
John Stevens,
Safa AlSarraj,
Stuart PickeringBrown,
John Hardy,
Nick C. Fox,
John Collinge,
Elizabeth K. Warrington,
Martin N. Rossor
Publication year - 2008
Publication title -
archives of neurology
Language(s) - English
Resource type - Journals
eISSN - 1538-3687
pISSN - 0003-9942
DOI - 10.1001/archneur.65.4.506
Subject(s) - frontotemporal lobar degeneration , frontotemporal dementia , aphasia , atrophy , parietal lobe , psychology , primary progressive aphasia , neuroscience , medicine , pathology , dementia , disease
To describe the clinical, neuropsychologic, and radiologic features of a family with a C31LfsX35 mutation in the progranulin gene CCDS11483.1).
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