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In-depth phenotypic description of TBK1 mutations ; a frequent cause of FTD and ALS in the Flanders-Belgian population
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Extensive genetic and phenotypic description of MAPT p.R406W in the Flanders-Belgian population
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- Journal Article
- A1
- open access
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
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A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD
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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21