Mutation profile of APP, PSEN1, and PSEN2 in Chinese familial Alzheimer's disease
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DOI: 10.1016/j.neurobiolaging.2019.01.018
Abstract: Causative mutations in the genes encoding amyloid precursor protein (APP), presenilin 1 (PSEN1), or presenilin 2 (PSEN2) account for a majority of cases of familial Alzheimer disease (FAD) inherited in an autosomal-dominant pattern. For the… read more here.
Keywords: psen1 psen2; alzheimer disease; app psen1; familial alzheimer ... See more keywords