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Fig. 2 | Acta Neuropathologica Communications

Fig. 2

From: Rare missense mutations in ABCA7 might increase Alzheimer’s disease risk by plasma membrane exclusion

Fig. 2

Co-segregation of ABCA7 p.G1820S with AD. To respect the privacy of the participants, the sex of each person is masked, and the pedigree is scrambled. The black arrow indicates the proband. Slashed symbols indicate deceased individuals. Black diamonds indicate individuals diagnosed with AD. Diamonds with question marks represent individuals with hearsay AD. An asterisk represents participants of whom genomic DNA is available. A red ‘c’ represents (obligate) carriers of the ABCA7 p.G1820S mutation. The shared haplotype of the p.G1820S carriers is indicated in blue. AAO, age at onset; AAI, age at inclusion

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Acta Neuropathologica Communications

ISSN: 2051-5960

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