A novel GRN mutation in an Italian patient with non-fluent variant of primary progressive aphasia at onset: a longitudinal case report

OBJECTIVES: We report the clinical presentation and evolution of a case with a novel Progranulin gene (GRN) mutation and non-fluent language disturbances at onset. MATERIALS AND METHODS: A 60 year-old, white patient was followed due to a history of language disturbances. Eighteen months after onset,...

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Detalles Bibliográficos
Autores principales: Castelnovo, Veronica, Canu, Elisa, Domi, Teuta, Pozzi, Laura, Vignaroli, Francesca, Spinelli, Edoardo Gioele, Ghirelli, Alma, Tondo, Giacomo, Comi, Cristoforo, Riva, Nilo, Quattrini, Angelo, Carrera, Paola, Filippi, Massimo, Agosta, Federica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296183/
https://www.ncbi.nlm.nih.gov/pubmed/37383099
http://dx.doi.org/10.3389/fnins.2023.1204504

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296183/
https://www.ncbi.nlm.nih.gov/pubmed/37383099
http://dx.doi.org/10.3389/fnins.2023.1204504

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