Alzheimer's Disease-Like Phenotype Associated With the c.154delA Mutation in Progranulin

OBJECTIVE: To characterize a kindred with a familial neurodegenerative disorder associated with a mutation in progranulin (PGRN), emphasizing the unique clinical features in this kindred. DESIGN: Clinical, radiologic, pathologic, and genetic characterization of a kindred with a familial neurodegener...

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Detalhes bibliográficos
Main Authors: Kelley, Brendan J., Haidar, Wael, Boeve, Bradley F., Baker, Matt, Shiung, Maria, Knopman, David S., Rademakers, Rosa, Hutton, Mike, Adamson, Jennifer, Kuntz, Karen M., Dickson, Dennis W., Parisi, Joseph E., Smith, Glenn E., Petersen, Ronald C.
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2902004/
https://ncbi.nlm.nih.gov/pubmed/20142525
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archneurol.2010.113
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