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The causes of phenotypic heterogeneity in familial Alzheimer’s disease with autosomal dominant inheritance are not well understood. We aimed to characterise clinical phenotypes and genetic associations with APP and PSEN1 mutations in symptomatic autosomal dominant familial Alzheimer’s disease (ADAD).

More information Original publication

DOI

https://doi.org/10.1016/S1474-4422(16)30193-4

Type

Journal article

Publisher

Elsevier

Publication Date

12/2016

Volume

15