Ahmed, S; Fairen, MD; Sabir, MS; Pastor, P; Ding, J; Ispierto, L; Butala, A; ... Scholz, SW; + view all Ahmed, S; Fairen, MD; Sabir, MS; Pastor, P; Ding, J; Ispierto, L; Butala, A; Morris, CM; Schulte, C; Gasser, T; Jabbari, E; Pletnikova, O; Morris, HR; Troncoso, J; Gelpi, E; Pantelyat, A; Scholz, SW; - view fewer (2019) MAPT p.V363I mutation: A rare cause of corticobasal degeneration. Neurology Genetics , 5 (4) , Article e347. 10.1212/NXG.0000000000000347.