Log in to save to my catalogue

Argyrophilic grain disease: molecular genetic difference to other four-repeat tauopathies

Argyrophilic grain disease: molecular genetic difference to other four-repeat tauopathies

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_75710082

Argyrophilic grain disease: molecular genetic difference to other four-repeat tauopathies

About this item

Full title

Argyrophilic grain disease: molecular genetic difference to other four-repeat tauopathies

Publisher

Berlin: Springer

Journal title

Acta neuropathologica, 2003-10, Vol.106 (4), p.363-366

Language

English

Formats

Publication information

Publisher

Berlin: Springer

More information

Scope and Contents

Contents

Argyrophilic grain disease (AgD) is a four-repeat tauopathy that is almost exclusively restricted to allocortical areas. Progressive supranuclear palsy and corticobasal degeneration also show predominant deposition of four-repeat tau filaments, and are associated with the tau H1 haplotype. We investigated a possible association between AgD and the...

Alternative Titles

Full title

Argyrophilic grain disease: molecular genetic difference to other four-repeat tauopathies

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_75710082

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_75710082

Other Identifiers

ISSN

0001-6322

E-ISSN

1432-0533

DOI

10.1007/s00401-003-0742-x

How to access this item