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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Autori principali: 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
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2011
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Accesso online: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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