Publication | Open Access
A Presenilin 1 Mutation Associated with Familial Frontotemporal Dementia Inhibits γ-Secretase Cleavage of APP and Notch
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2002
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Neurodegenerative DiseasesGenetic DisorderDementiaGeneticsMutation AssociatedDegenerative DiseaseDegenerative PathologyFrontotemporal DementiaNeurologyNeurodegenerationMedicinePresenilin 1Neurogenetics
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