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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
Atypical progressive supranuclear palsy with corticospinal tract degeneration
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
