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Fig. 1 | Acta Neuropathologica Communications

Fig. 1

From: Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene

Fig. 1

Pedigree of family PED.25. The family segregates the SORL1 variant c.3907C > T (p.Arg1303Cys) in two generations. Individuals included in the whole-exome sequencing (WES) are marked with an *. The genetic status for variant c.3907C > T is indicated “carrier” for heterozygotes, “wildtype” when absent, and “unknown” if DNA was unavailable. Diagnosis refers to the clinical diagnosis. Onset refers to first observation of dementia symptoms, and APOE indicates the ε-alleles. Neuropath indicates the post mortem neuropathological diagnosis. The age at last known affection status of individuals still alive is indicated in parenthesis

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Acta Neuropathologica Communications

ISSN: 2051-5960

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