MAPT p.V363I mutation: A rare cause of corticobasal degeneration.
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.
Ahmed S, et al. Among authors: pletnikova o.
Neurol Genet. 2019 Jun 25;5(4):e347. doi: 10.1212/NXG.0000000000000347. eCollection 2019 Aug.
Neurol Genet. 2019.
PMID: 31404212
Free PMC article.