Li QS, Tian C, 23andMe Research Team, Hinds D, Seabrook GR. The association of clinical phenotypes to known AD/FTD genetic risk loci and their inter-relationship. PLoS One. 2020;15(11):e0241552. Epub 2020 Nov 5 PubMed.

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Mutations

  1. APOE C130R (ApoE4)
  2. APOE R176C (ApoE2)