Article
Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene.
Archives of neurology - 1 Apr 2008
Rohrer Jonathan D, Warren Jason D, Omar Rohani, Mead Simon, Beck Jonathan, Revesz Tamas, Holton Janice, Stevens John M, Al-Sarraj Safa, Pickering-Brown Stuart M, Hardy John, Fox Nick C, Collinge John, Warrington Elizabeth K, Rossor Martin N
Abstract excerpt
OBJECTIVE: To describe the clinical, neuropsychologic, and radiologic features of a family with a C31LfsX35 mutation in the progranulin gene CCDS11483.1). DESIGN: Case series. PATIENTS: A large British kindred (DRC255) with a PGRN mutation was assessed. Affected individuals presented with a mean age of 57.8 years (range, 54-67 years) and a mean disease duration of 6.1 years (range, 2-11 years). RESULTS: All...
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