One novel GRN null mutation, two different aphasia phenotypes
Author:
Publisher
Elsevier BV
Subject
Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience
Reference40 articles.
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1. A novel GRN mutation in an Italian patient with non-fluent variant of primary progressive aphasia at onset: a longitudinal case report;Frontiers in Neuroscience;2023-06-13
2. Genetic forms of primary progressive aphasia within the GENetic Frontotemporal dementia Initiative (GENFI) cohort: comparison with sporadic primary progressive aphasia;Brain Communications;2023-02-17
3. FTD-PSP is an Unusual Clinical Phenotype in A Frontotemporal Dementia Patient with A Novel Progranulin Mutation;Aging and disease;2021
4. OUP accepted manuscript;Brain;2021
5. The Rise of the GRN C157KfsX97 Mutation in Southern Italy: Going Back to the Fall of the Western Roman Empire;Journal of Alzheimer's Disease;2020-10-27
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