Fig. 2From: Comprehensive genetic screening of early-onset dementia patients in an Austrian cohort-suggesting new disease-contributing genesThe bar graph shows the relative frequency of strong FH (Goldman score 1–2), moderate to low FH (3–3.5) and negative or unknown FH (4–4.5) in patients with autosomal dominant variants (a.d.; PSEN1, MAPT, APP duplication/missense mutation, GRN), APOE4/4: Homozygote APOE4 carriers; risk variant: well-established risk variants (TREM2, APOE4) and no variants in established risk genes or of unknown significanceBack to article page