Clinical findings in nondemented mutation carriers predisposed to Alzheimer's disease: a model of mild cognitive impairment
Author:
Publisher
Wiley
Subject
Clinical Neurology,Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1600-0404.107.s179.11.x/fullpdf
Reference24 articles.
1. Amyloid, presenilins and Alzheimer's disease;Hardy;Trends Neurosci,1997
2. A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of β-amyloid;Mullan;Nat Genet,1992
3. The ‘Arctic’ mutation (E693G) causes Alzheimer's disease by enhanced Abeta protoformation protofibril formation;Nilsberth;Nat Neurosci,2001
4. Chromosome 14-encoded Alzheimer's disease: genetic and clinicopathological description;Haltia;Arch Neurol,1994
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