Mutation screening in Chinese patients with familial Alzheimer's disease by whole-exome sequencing
Abstract
Familial Alzheimer's disease (FAD) is characterized by a positive family history of dementia and typically occurs at an early age with an autosomal dominant pattern of inheritance. Amyloid precursor protein (APP), presenilin1 (PSEN1), and presenilin2 (PSEN2) are the major causative genes of FAD. The spectrum of mutations in patients with FAD has been investigated extensively in the Caucasian population but rarely in the Chinese population. Here,...
Paper Details
Title
Mutation screening in Chinese patients with familial Alzheimer's disease by whole-exome sequencing
Published Date
Apr 1, 2019
Journal
Volume
76
Pages
215.e15 - 215.e21
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