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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429247/
https://www.ncbi.nlm.nih.gov/pubmed/28529873
http://dx.doi.org/10.1016/j.nicl.2017.04.015

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5429247/
https://www.ncbi.nlm.nih.gov/pubmed/28529873
http://dx.doi.org/10.1016/j.nicl.2017.04.015

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