A Novel GRN Mutation (GRN c.708+6_+9delTGAG) in Frontotemporal Lobar Degeneration with TDP-43-positive Inclusions: Clinicopathologic Report of 6 Cases

Understanding of frontotemporal lobar degeneration (FTLD), the underlying pathology that is most often linked to the clinical diagnosis of frontotemporal dementia (FTD), is rapidly increasing. Mutations in 7 known genes (MAPT, GRN, C9orf72, VCP, CHMP2B, and rarely TARDBP and FUS) are associated with...

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Huvudupphovsmän: Bit-Ivan, Esther N., Suh, Eunran, Shim, H-S, Weintraub, Sandra, Hyman, Bradley T., Arnold, Steven E., McCarty-Wood, Elisabeth, Van Deerlin, Viviana M., Schneider, Julie A., Trojanowski, John Q., Frosch, Matthew P., Baker, Matt C., Rademakers, Rosa, Mesulam, Marsel, Bigio, Eileen H.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2014
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC4109801/
https://ncbi.nlm.nih.gov/pubmed/24709683
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/NEN.0000000000000070
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