Skip to main content
. 2023 Aug 29;14:1239725. doi: 10.3389/fneur.2023.1239725

Figure 2.

Figure 2

Selected pedigrees (genotyping only performed in probands). (A) Family of proband (fam_006) with heterozygous MFN2 mutation. (B) Family of proband (fam_111) with novel PSEN1 mutation presenting with spastic paraparesis (SP) followed by progressive aphasia (PA).