White matter hyperintensities are seen only in GRN mutation carriers in the GENFI cohort

Genetic frontotemporal dementia is most commonly caused by mutations in the progranulin (GRN), microtubule-associated protein tau (MAPT) and chromosome 9 open reading frame 72 (C9orf72) genes. Previous small studies have reported the presence of cerebral white matter hyperintensities (WMH) in geneti...

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Опубликовано в: :Neuroimage Clin
Главные авторы: Sudre, Carole H., Bocchetta, Martina, Cash, David, Thomas, David L., Woollacott, Ione, Dick, Katrina M., van Swieten, John, Borroni, Barbara, Galimberti, Daniela, Masellis, Mario, Tartaglia, Maria Carmela, Rowe, James B., Graff, Caroline, Tagliavini, Fabrizio, Frisoni, Giovanni, Laforce, Robert, Finger, Elizabeth, de Mendonça, Alexandre, Sorbi, Sandro, Ourselin, Sébastien, Cardoso, M. Jorge, Rohrer, Jonathan D.
Формат: Artigo
Язык:Inglês
Опубликовано: Elsevier 2017
Предметы:
Regular Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC5429247/
https://ncbi.nlm.nih.gov/pubmed/28529873
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2017.04.015
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