Coexistent Tau and Amyloid Pathology in Hereditary Frontotemporal Dementia with Tau Mutations
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.2000.tb06912.x/fullpdf
Reference20 articles.
1. Frontotemporal lobar degeneration;Neary;A consensus on clinical diagnostic criteria. Neurology,1998
2. Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus statement;Foster;Ann. Neurol.,1997
3. Tau is a candidate gene for chromosome 17 frontotemporal dementia;Poorkaj;Ann. Neurol.,1998
4. Coding and splice-donor site mutations in tau cause inherited dementia (FTDP-17);Hutton;Nature,1998
5. Mutation in the tau gene in familial multiple system tauopathy with presenile dementia;Spillantini;Proc. Natl. Acad. Sci. USA,1998
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