SORL1 variants across Alzheimer's disease European American cohorts

The accumulation of the toxic Aβ peptide in Alzheimer's disease (AD) largely relies upon an efficient recycling of amyloid precursor protein (APP). Recent genetic association studies have described rare variants in SORL1 with putative pathogenic consequences in the recycling of APP. In this wor...

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Veröffentlicht in:European journal of human genetics : EJHG 2016-12, Vol.24 (12), p.1828-1830
Hauptverfasser: Fernández, Maria Victoria, Black, Kathleen, Carrell, David, Saef, Ben, Budde, John, Deming, Yuetiva, Howells, Bill, Del-Aguila, Jorge L, Ma, Shengmei, Bi, Catherine, Norton, Joanne, Chasse, Rachel, Morris, John, Goate, Alison, Cruchaga, Carlos
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Sprache:eng
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Zusammenfassung:The accumulation of the toxic Aβ peptide in Alzheimer's disease (AD) largely relies upon an efficient recycling of amyloid precursor protein (APP). Recent genetic association studies have described rare variants in SORL1 with putative pathogenic consequences in the recycling of APP. In this work, we examine the presence of rare coding variants in SORL1 in three different European American cohorts: early-onset, late-onset AD (LOAD) and familial LOAD.
ISSN:1018-4813
1476-5438
DOI:10.1038/ejhg.2016.122