Associated Papers
Rare variant aggregation in 148,508 exomes identifies genes associated with proxy dementia.
Wightman DP et al.
Scientific Reports, 2023
36750708 (PubMed )
Supplement: 41598_2023_29108_MOESM1_ESM.xlsx › Supp_T11
Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer's disease.
Schulte EC et al.
Human Genome Variation, 2015
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