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Alternative splicing in a presenilin 2 variant associated with Alzheimer disease.

Annals of clinical and translational neurology | 2019

Autosomal-dominant familial Alzheimer disease (AD) is caused by by variants in presenilin 1 (PSEN1), presenilin 2 (PSEN2), and amyloid precursor protein (APP). Previously, we reported a rare PSEN2 frameshift variant in an early-onset AD case (PSEN2 p.K115Efs*11). In this study, we characterize a second family with the same variant and analyze cellular transcripts from both patient fibroblasts and brain lysates.

Pubmed ID: 31020001 RIS Download

Associated grants

  • Agency: NIA NIH HHS, United States
    Id: P50 AG005136
  • Agency: NIA NIH HHS, United States
    Id: T32 AG052354

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