A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease
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Updated: Oct 2, 2026

In Vitro Aggregation Assays Using Hyperphosphorylated Tau Protein
Published on: January 2, 2015
Sonia M Rosso1, Esther van Herpen, Wout Deelen
1Department of Neurology, Erasmus Medical Center, Rotterdam, The Netherlands.
Abstract:
Mutations in the tau gene cause familial frontotemporal dementia and parkinsonism linked to chromosome 17. In this article, we describe a novel missense mutation, S320F, in the tau gene in a family with presenile dementia. To our knowledge, it is the first mutation to be described in exon 11 of tau. The proband died at age 53 years, after a disease duration of 15 years, and autopsy revealed a neuropathological picture similar to Pick's disease. Recombinant tau protein with the S320F mutation showed a greatly reduced ability to promote microtubule assembly.
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