Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study
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 o...
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Veröffentlicht in: | Lancet neurology 2020-02, Vol.19 (2), p.145-156 |
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Format: | Artikel |
Sprache: | eng |
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