Associated Papers
Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementia.
Miedema SSM et al.
Acta Neuropathologica Communications, 2022
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study.
Moore KM et al.
The Lancet. Neurology, 2020
31810826 (PubMed )
Supplement: NIHMS1067362-supplement-Supplement.pdf
Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.
Dopper EG et al.
Journal of Molecular Neuroscience : Mn, 2011
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