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. MAPT p.V363I mutation: A rare cause of corticobasal degeneration. Neurol Genet. 2019 Aug;5(4):e347. Epub 2019 Jun 25 PubMed.
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