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Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease

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Schott, Jonathan | Crutch, Sebastian | Carrasquillo, Minerva | Uphill, James | Shakespeare, Tim | Ryan, Natalie | Yong, Keir | Lehmann, Manja | Ertekin-Taner, Nilufer | Graff-Radford, Neill | Boeve, Bradley | Murray, Melissa | Khan, Qurat Ul Ain | Petersen, Ronald | Dickson, Dennis | Knopman, David | Rabinovici, Gil | Miller, Bruce | González, Aida Suárez | Gil-Néciga, Eulogio | Snowden, Julie | Harris, Jenny | Pickering-Brown, Stuart | Louwersheimer, Eva | van Der Flier, Wiesje | Scheltens, Philip | Pijnenburg, Yolande | Galasko, Douglas | Sarazin, Marie | Dubois, Bruno | Magnin, Eloi | Galimberti, Daniela | Scarpini, Elio | Cappa, Stefano | Hodges, John | Halliday, Glenda | Bartley, Lauren | Carrillo, Maria | Bras, Jose | Hardy, John | Rossor, Martin | Collinge, John | Fox, Nick | Mead, Simon | Ertekin‐taner, Nilufer | Graff‐radford, Neill | Gil‐néciga, Eulogio | Pickering‐brown, Stuart | Flier, Wiesje

Edité par CCSD ; Alzheimer's Association / Wiley -

International audience. The genetics underlying posterior cortical atrophy (PCA), typically a rare variant of Alzheimer's disease (AD), remain uncertain.

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