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. Author manuscript; available in PMC: 2016 Jan 1.
Published in final edited form as: Neurobiol Aging. 2014 Aug 1;36(1):545.e9–545.e14. doi: 10.1016/j.neurobiolaging.2014.07.038

Figure 1.

Figure 1

Diagrams of three Italian families affected by Alzheimer’s Disease, in which mutations were identified by NeuroX. Genotypes are shown below the ID number with the mutant allele highlighted in bold font. Where available age at the time of examination is shown in the upper right corner and age of onset is indicated below the ID number. The gender of family members is masked to protect patient confidentiality. a) FLO25 with the PSEN1 p.M233T mutation (T>C). b) FLO61 with the rare ABCA7 p.L400V variant (C>G). c) FLO66 with the TREM2 p.D87N (G>A).