Novel missense progranulin gene mutation associated with the semantic variant of primary progressive aphasia.

Abstract

Progranulin (GRN) mutations are typically associated with the behavioral variant of frontotemporal dementia and the non-fluent variant of primary progressive aphasia phenotypes. Hereby, we describe a patient affected by semantic variant of primary progressive aphasia (svPPA) with a highly positive family history of dementia, carrying a novel GRN missense… (More)
DOI: 10.3233/JAD-130317

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Cite this paper

@article{Cerami2013NovelMP, title={Novel missense progranulin gene mutation associated with the semantic variant of primary progressive aphasia.}, author={Chiara Cerami and Alessandra Marcone and D Galimberti and Chiara Villa and Chiara Fenoglio and Elio Angelo Scarpini and Stefano F. Cappa}, journal={Journal of Alzheimer's disease : JAD}, year={2013}, volume={36 3}, pages={415-20} }