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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases. [electronic resource] by
Producer: 20130625 In: Human molecular genetics vol. 21
Availability: No items available.

174.
Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials. [electronic resource] by
Producer: 20160513 In: JAMA neurology vol. 73
Availability: No items available.

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Rarity of the Alzheimer disease-protective APP A673T variant in the United States. [electronic resource] by
Producer: 20150415 In: JAMA neurology vol. 72
Availability: No items available.

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Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study. [electronic resource] by
Producer: 20150304 In: JAMA neurology vol. 71
Availability: No items available.

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Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. [electronic resource] by
Producer: 20171025 In: Nature genetics vol. 49
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Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. [electronic resource] by
Producer: 20190424 In: Nature genetics vol. 51
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179.
Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. [electronic resource] by
Publication details: Nature genetics Sep 2019
In: Nature genetics vol. 51
Availability: No items available.

180.
Guidelines for the use and interpretation of assays for monitoring autophagy. [electronic resource] by
Producer: 20121106 In: Autophagy vol. 8
Availability: No items available.