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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
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The molecular genetics of early-onset Alzheimer's disease
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Mutation analysis of candidate genes for chromosome 17-linked tau-negative FTD
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Neuropathological and biochemical characterization of a familial FTD patient carrying PS1 GLY183VAL
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Possible association of nicastrin polymorphisms and Alzheimer disease in the Finnish population
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Octapeptide repeat insertions in the prion protein gene and early onset dementia
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A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression
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Hot-spot residue in small heat-shock protein 22 causes distal motor neuropathy
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A straightforward approach to evaluate false positive associations in studies of gene interaction
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Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in western Europe