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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2011
Aiheet:
Article
Linkit: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
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!

Samankaltaisia teoksia