PRION PROTEIN CODON 129 POLYMORPHISM MODIFIES AGE AT ONSET OF FRONTOTEMPORAL DEMENTIA WITH THE C.709-1G>A PROGRANULIN MUTATION

Frontotemporal lobar degeneration due to mutations in the progranulin gene (PGRN) presents a high variability both in the clinical phenotype and age of onset of disease. Factors that influence this variability remain largely unknown. The aim of our study was to determine whether selected genetic var...

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Bibliografiske detaljer
Main Authors: Moreno, Fermín, Alzualde, Ainhoa, Camblor, Pablo Martínez, Barandiaran, Myriam, Van Deerlin, Vivianna M., Gabilondo, Alazne, Martí Massó, José F., de Munain, Adolfo López, Indakoetxea, Begoña
Format: Artigo
Sprog:Inglês
Udgivet: 2011
Fag:
Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3540994/
https://ncbi.nlm.nih.gov/pubmed/20711061
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WAD.0b013e3181eff695
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