Frontotemporal dementia and Parkinsonism linked to chromosome 17 in a young Australian patient with the G389R Tau mutation
Author:
Publisher
Wiley
Subject
Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2990.2007.00918.x/fullpdf
Reference22 articles.
1. Frontotemporal lobar degeneration: A consensus on clinical diagnostic criteria
2. Phenotypic correlations in FTDP-17
3. TauGene Mutation G389R Causes a Tauopathy with Abundant Pick Body-like Inclusions and Axonal Deposits
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