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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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Detalhes bibliográficos
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
Formato: Artigo
Idioma:Inglês
Publicado em: 2011
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Acesso em linha: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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