Clinical and Molecular Characterization of a Novel Progranulin Deletion Associated with Different Phenotypes
Articolo
Data di Pubblicazione:
2020
Abstract:
Background: Mutations in the GRN gene are causative for an autosomal dominant form of frontotemporal dementia.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Dementia; gene; genetics; parkinsonism; progranulin; progressive supranuclear palsy
Elenco autori:
Vitale, Emilia
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