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[Twenty-one unrelated patients with a history of suspected familial Alzheimer disease (FAD) were screened for mutations in PSEN1, PSEN2, and APP, the known FAD genes encoding the presenilins (PS1 and PS2) and the amyloid precursor protein (APP).The mutation detection rate was 57%.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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