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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: 2006
Matèries:
Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars