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Extended FTLD pedigree segregating a Belgian GRN-null mutation : neuropathological heterogeneity in one family
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- Journal Article
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Clinical variability and onset age modifiers in an extended Belgian GRN founder family
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Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
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Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion
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TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis
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Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
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Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
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Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains
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Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration