Progressive supranuclear palsy-like phenotype caused by progranulin p.Thr272fs mutation
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.23749/fullpdf
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3. Clinical features and diagnosis of frontotemporal dementia;Kertesz;Front Neurol Neurosci,2009
4. Refining frontotemporal dementia with parkinsonism linked to chromosome 17: introducing FTDP-17 (MAPT) and FTDP-17 (PGRN);Boeve;Arch Neurol,2008
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