Gatto EM, Allegri RF, Da Prat G, Chrem Mendez P, Hanna DS, Dorschner MO, Surace EI, Zabetian CP, Mata IF. Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: first report in South America. Neurobiol Aging. 2017 May;53:195.e11-195.e17. Epub 2017 Feb 10 PubMed.

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Mutations

  1. MAPT P301L