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The gene encoding nicastrin, a major gamma-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sampleDigenic progressive external ophthalmoplegia in a sporadic patient: recessive mutations in POLG and C10orf2/TwinkleEarly cognitive decline is associated with prion protein codon 129 polymorphismNull mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21Tau phosphorylation regulates the interaction between BIN1's SH3 domain and Tau's proline-rich domainDevelopmental Expression of 4-Repeat-Tau Induces Neuronal Aneuploidy in Drosophila Tauopathy ModelsRare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degenerationTBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.
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P50
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