APA (7th ed.) Citation

(2017). Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: First report in South America.

Chicago Style (17th ed.) Citation

Intrafamilial Variable Phenotype Including Corticobasal Syndrome in a Family with P.P301L Mutation in the MAPT Gene: First Report in South America. 2017.

MLA (8th ed.) Citation

Intrafamilial Variable Phenotype Including Corticobasal Syndrome in a Family with P.P301L Mutation in the MAPT Gene: First Report in South America. 2017.