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Variant of TREM2 Associated with the Risk of Alzheimer's Disease

by: Thorlakur Jonsson, Hreinn Stefansson, Stacy Steinberg, Ingileif Jonsdottir, Palmi V. Jonsson, Jon Snaedal, Sigurbjorn Bjornsson, Johanna Huttenlocher, Allan I. Levey, James J. Lah, Dan Rujescu, Harald Hampel, Ina Giegling, Ole A. Andreassen, Knut Engedal, Ingun Ulstein, Srdjan Djurovic, Carla Ibrahim-Verbaas, Albert Hofman, M. Arfan Ikram, Cornelia M. van Duijn, Unnur Thorsteinsdottir, Augustine Kong, Kari Stefansson
N Engl J Med In New England Journal of Medicine, Vol. 368, No. 2. (14 November 2012), pp. 107-116, doi:10.1056/nejmoa1211103  Key: citeulike:11701357

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Abstract

Alzheimer's disease, the most common form of dementia in the elderly, is a neurodegenerative disorder that is characterized by a slow but progressive loss of cognitive function. Extracellular amyloid plaques, intracellular neurofibrillary tangles, and loss of neurons and synapses resulting in brain atrophy are the main pathological hallmarks of Alzheimer's disease.1 Disease onset is usually after the age of 70 years, although the prevalence increases exponentially with age after the age of 65 years and exceeds 25% in those over the age of 90 years.2 The vast majority of variants in the sequence of the genome that have been shown . . .


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