Polygenic variants related to familial hypobetalipoproteinemia in a patient with Alzheimer's disease homozygotic for the APOE ε2 allele presenting multiple cortical superficial siderosis and recurrent lobar hemorrhages

Neurogenetics. 2022 Jan;23(1):69-71. doi: 10.1007/s10048-021-00672-3. Epub 2021 Oct 2.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Alzheimer Disease* / complications
  • Alzheimer Disease* / genetics
  • Apolipoprotein E2 / genetics
  • Hemorrhage
  • Humans
  • Hypobetalipoproteinemias*
  • Siderosis*

Substances

  • Apolipoprotein E2