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2016
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2012
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2015
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Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sites.
Not available
S-EPMC3265835
|
biostudies-literature
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The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter.
Not available
S-EPMC4960451
|
biostudies-literature
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Both common variations and rare non-synonymous substitutions and small insertion/deletions in CLU are associated with increased Alzheimer risk.
Not available
S-EPMC3296573
|
biostudies-literature
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Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation.
Not available
S-EPMC4917260
|
biostudies-literature
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Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort.
Not available
S-EPMC4691687
|
biostudies-literature
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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.
Not available
S-EPMC4131163
|
biostudies-literature
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