Cite
P1‐286: A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia
MLA
Elisa Ridolfi, et al. “P1‐286: A Novel MAPT Mutation Associated with the Clinical Phenotype of Progressive Nonfluent Aphasia.” Alzheimer’s & Dementia, vol. 7, July 2011. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi...........97c26771995375bd375070ffef1e2ef5&authtype=sso&custid=ns315887.
APA
Elisa Ridolfi, Luisa Benussi, Andrea Arighi, Elio Scarpini, Alessandra Marcone, A. Mandelli, Chiara Fenoglio, Maria Serpente, Francesca Cortini, Stefano F. Cappa, Giuliano Binetti, Anna M. Pietroboni, Nereo Bresolin, Giorgio G. Fumagalli, Francesca Jacini, Chiara Villa, Roberta Ghidoni, Laura Ghezzi, Claudia Cantoni, & Daniela Galimberti. (2011). P1‐286: A novel MAPT mutation associated with the clinical phenotype of progressive nonfluent aphasia. Alzheimer’s & Dementia, 7.
Chicago
Elisa Ridolfi, Luisa Benussi, Andrea Arighi, Elio Scarpini, Alessandra Marcone, A. Mandelli, Chiara Fenoglio, et al. 2011. “P1‐286: A Novel MAPT Mutation Associated with the Clinical Phenotype of Progressive Nonfluent Aphasia.” Alzheimer’s & Dementia 7 (July). http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi...........97c26771995375bd375070ffef1e2ef5&authtype=sso&custid=ns315887.