Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
Abstract
Frontotemporal dementia is a heterogenous neurodegenerative disorder, with about a third of cases being genetic. Most of this genetic component is accounted for by mutations in GRN, MAPT, and C9orf72. In this study, we aimed to complement previous phenotypic studies by doing an international study of age at symptom onset, age at death, and disease duration in individuals with mutations in GRN, MAPT, and C9orf72.In this international,...
Paper Details
Title
Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
Published Date
Feb 1, 2020
Journal
Volume
19
Issue
2
Pages
145 - 156
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