Prion protein amyloidosis with divergent phenotype associated with two novel nonsense mutations in PRNP.Comprehensive mRNA expression profiling distinguishes tauopathies and identifies shared molecular pathways.A second class of Gerstmann-Straussler-Scheinker disease linked to the G131V mutation in the prion protein gene in a Dutch patient.Three VCP mutations in patients with frontotemporal dementia.
author
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J.C. Van Swieten
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Van Swieten