Characteristics of Frontotemporal Dementia Patients with a Progranulin Mutation

OBJECTIVE: Mutations in the Progranulin gene (PGRN) recently have been discovered to be associated with frontotemporal dementia (FTD) linked to 17q21 without identified MAPT mutations. The range of mutations of PGRN that can result in the FTD phenotype and the clinical presentation of patients with...

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Hlavní autoři: Huey, Edward D., Grafman, Jordan, Wassermann, Eric M., Pietrini, Pietro, Tierney, Michael C., Ghetti, Bernardino, Spina, Salvatore, Baker, Matt, Hutton, Mike, Elder, Joshua W., Berger, Stephen L., Heflin, Kyle A., Hardy, John, Momeni, Parastoo
Médium: Artigo
Jazyk:Inglês
Vydáno: 2006
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On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2987739/
https://ncbi.nlm.nih.gov/pubmed/16983677
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.20969
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