MAPT p.V363I mutation: A rare cause of corticobasal degeneration

por Ahmed, Sarah, Fairen, Monica Diez, Sabir, Marya S., Pastor, Pau, Ding, Jinhui, Ispierto, Lourdes, Butala, Ankur, Morris, Christopher M., Schulte, Claudia, Gasser, Thomas, Jabbari, Edwin, Pletnikova, Olga, Morris, Huw R., Troncoso, Juan, Gelpi, Ellen, Pantelyat, Alexander, Scholz, Sonja W.
Publicado 2019