Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degeneration
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2008.02272.x/fullpdf
Reference21 articles.
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3. Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia;Poorkaj;Archives of Neurology,2001
4. Frontotemporal dementia in the Netherlands: patient characteristics and prevalence estimates from a population-based study;Rosso;Brain,2003
5. Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations;Pickering-Brown;Brain,2008
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