APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases

“APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases” has been published in the journal PLOS Medicine. This work was supported in part by JPND through the PERADES project, selected in the 2012 risk factors call.