A novel V272D presenilin mutation associated with logopenia, disorientation, and apraxia in an autosomal-dominant Alzheimer's disease family

Published 2019 View Full Article

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Title
A novel V272D presenilin mutation associated with logopenia, disorientation, and apraxia in an autosomal-dominant Alzheimer's disease family
Authors
Keywords
Early-onset Alzheimer's disease, PSEN1 mutation, APP, Amyloid-β 42/40 ratio, Neurocognitive disorder
Journal
NEUROBIOLOGY OF AGING
Volume -, Issue -, Pages -
Publisher
Elsevier BV
Online
2019-08-07
DOI
10.1016/j.neurobiolaging.2019.07.002

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