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Dive into the research topics of 'MAPT p.V363I mutation A rare cause of corticobasal degeneration'. Together they form a unique fingerprint.- Sort by
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Sarah Ahmed, Monica Diez Fairen, Marya S. Sabir, Pau Pastor, Jinhui Ding, Lourdes Ispierto, Ankur Butala, Christopher M. Morris, Claudia Schulte, Thomas Gasser, Edwin Jabbari, Olga Pletnikova, Huw R. Morris, Juan Troncoso, Ellen Gelpi, Alexander Pantelyat, Sonja W. Scholz
Research output: Contribution to journal › Article › peer-review