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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Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2010
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Article
Accesso online: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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