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Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders
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Shortcutting the diagnostic odyssey : the multidisciplinary program for undiagnosed rare diseases in adults (UD-PrOZA)
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Loss of DPP6 in neurodegenerative dementia : a genetic player in the dysfunction of neuronal excitability
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No supportive evidence for TIA1 gene mutations in a European cohort of ALS-FTD spectrum patients
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An intronic VNTR affects splicing of ABCA7 and increases risk of Alzheimer's disease
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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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TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis
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Investigating the role of ALS genes CHCHD10 and TUBA4A in Belgian FTD-ALS spectrum patients
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Clinical evidence of disease anticipation in families segregating a C9orf72 repeat expansion