A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.

Article Details

Citation

Rosso SM, van Herpen E, Deelen W, Kamphorst W, Severijnen LA, Willemsen R, Ravid R, Niermeijer MF, Dooijes D, Smith MJ, Goedert M, Heutink P, van Swieten JC

A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.

Ann Neurol. 2002 Mar;51(3):373-6.

PubMed ID
11891833 [ View in PubMed
]
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.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Microtubule-associated protein tauP10636Details