Parietal Lobe Deficits in Frontotemporal Lobar Degeneration Caused by a Mutation in the Progranulin Gene

OBJECTIVE: To describe the clinical, neuropsychological and radiological features of a family with a C31LfsX35 mutation in the progranulin gene (PGRN). DESIGN: Case series PATIENTS: A large British kindred (DRC255) with a PGRN mutation was assessed. Affected individuals presented with a mean age of...

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Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2578869/
https://ncbi.nlm.nih.gov/pubmed/18413474
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneur.65.4.506
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