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
Frontotemporal dementia (FTD) is considered to have a heterogeneous aetiology. To date the tau gene ...
Frontotemporal dementia and parkinsonism linked to chromosome 17 have been associated with mutations...
Abundant cytoplasmic inclusions consisting of aggregated hyperphosphorylated protein tau a...
Recently, mutations within the tau gene have been associated with some familial forms of frontotempo...
Exonic and intronic mutations in Tau cause familial neurodegenerative syndromes characterized by fro...
AbstractRecently exonic and intronic mutations in the gene for microtubule-associated protein tau ha...
Exonic and intronic mutations in Tau cause familial neurodegenerative syndromes characterized by fro...
textabstractMutations in microtubule-associated protein tau recently have been identified in ...
SummaryMutations in microtubule-associated protein tau recently have been identified in familial cas...
Familial forms of frontotemporal dementia (FTD) with tauopathy are mostly caused by mutations in the...
Frontotemporal dementia (FTD) and Alzheimer's disease (AD) are two frequent causes of dementia that ...
AbstractAlzheimer’s disease is characterised by the degeneration of selected populations of nerve ce...
AbstractTau is the major component of the neurofibrillar tangles that are a pathological hallmark of...
Mutations in microtubule-associated protein tau re-cently have been identified in familial cases of ...
The majority of cases with frontotemporal dementia (FTD) have no tau deposition in the brain, yet mu...
Frontotemporal dementia (FTD) is considered to have a heterogeneous aetiology. To date the tau gene ...
Frontotemporal dementia and parkinsonism linked to chromosome 17 have been associated with mutations...
Abundant cytoplasmic inclusions consisting of aggregated hyperphosphorylated protein tau a...
Recently, mutations within the tau gene have been associated with some familial forms of frontotempo...
Exonic and intronic mutations in Tau cause familial neurodegenerative syndromes characterized by fro...
AbstractRecently exonic and intronic mutations in the gene for microtubule-associated protein tau ha...
Exonic and intronic mutations in Tau cause familial neurodegenerative syndromes characterized by fro...
textabstractMutations in microtubule-associated protein tau recently have been identified in ...
SummaryMutations in microtubule-associated protein tau recently have been identified in familial cas...
Familial forms of frontotemporal dementia (FTD) with tauopathy are mostly caused by mutations in the...
Frontotemporal dementia (FTD) and Alzheimer's disease (AD) are two frequent causes of dementia that ...
AbstractAlzheimer’s disease is characterised by the degeneration of selected populations of nerve ce...
AbstractTau is the major component of the neurofibrillar tangles that are a pathological hallmark of...
Mutations in microtubule-associated protein tau re-cently have been identified in familial cases of ...
The majority of cases with frontotemporal dementia (FTD) have no tau deposition in the brain, yet mu...
Frontotemporal dementia (FTD) is considered to have a heterogeneous aetiology. To date the tau gene ...
Frontotemporal dementia and parkinsonism linked to chromosome 17 have been associated with mutations...
Abundant cytoplasmic inclusions consisting of aggregated hyperphosphorylated protein tau a...