The progranulin (GRN) Cys157LysfsX97 mutation is associated with nonfluent variant of primary progressive aphasia clinical phenotype

Francesca Caso, Chiara Villa, Chiara Fenoglio, Roberto Santangelo, Federica Agosta, Elisabetta Coppi, Monica Falautano, Giancarlo Comi, Massimo Filippi, Elio Scarpini, Giuseppe Magnani, Daniela Galimberti

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