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29. Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: first report in South America. Gatto EM; Allegri RF; Da Prat G; Chrem Mendez P; Hanna DS; Dorschner MO; Surace EI; Zabetian CP; Mata IF Neurobiol Aging; 2017 May; 53():195.e11-195.e17. PubMed ID: 28268100 [TBL] [Abstract][Full Text] [Related]
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