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Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family
Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
Mild cognitive impairment
