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New insights into the genetic etiology of Alzheimer’s disease and related dementias
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease
Genome-wide association study of frontotemporal dementia identifies a C9ORF72 haplotype with a median of 12-G4C2 repeats that predisposes to pathological repeat expansions
Characterization of pathogenic SORL1 genetic variants for association with Alzheimer's disease: A clinical interpretation strategy
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