Gatto, E. M., Allegri, R. F., Da Prat, G., Chrem Mendez, P. A., Hanna, D. S., Dorschner, M. O., . . . Mata, I. F. (2016). Intrafamilial variable phenotype including corticobasal syndrome in a family with p.P301L mutation in the MAPT gene: First report in South America. Web
Citación estilo ChicagoGatto, Emilia Mabel, Ricardo Francisco Allegri, Gustavo Da Prat, Patricio Alexis Chrem Mendez, David S. Hanna, Michael O. Dorschner, Ezequiel Ignacio Surace, Cyrus P. Zabetian, and Ignacio F. Mata. Intrafamilial Variable Phenotype Including Corticobasal Syndrome in a Family With P.P301L Mutation in the MAPT Gene: First Report in South America. 2016.
Cita MLAGatto, Emilia Mabel, et al. Intrafamilial Variable Phenotype Including Corticobasal Syndrome in a Family With P.P301L Mutation in the MAPT Gene: First Report in South America. 2016.