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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
Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids
