Browsing by author "Majd, S"
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Dysregulation of Neuronal Iron Homeostasis as an Alternative Unifying Effect of Mutations Causing Familial Alzheimer’s Disease
Lumsden, AL; Rogers, JT; Majd, S; Newman, M; Sutherland, GT; Verdile, G; Lardelli, MPublished 2018-01-01The overwhelming majority of dominant mutations causing early onset familial Alzheimer's disease (EOfAD) occur in only three genes, PSEN1, PSEN2, and APP. An effect-in-common of these mutations is alteration of production ...Open AccessArticle
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