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emifad study group[Corporate Author]
(3 results)?
Whole-exome rare-variant analysis of Alzheimer's disease and related biomarker traits.
Alzheimers Dement. 2023 Jun;19(6):2317-2331. doi: 10.1002/alz.12842. Epub 2022 Dec 4.
Alzheimers Dement. 2023.
PMID: 36464806
Free article.
Rare variants in IFFO1, DTNB, NLRC3 and SLC22A10 associate with Alzheimer's disease CSF profile of neuronal injury and inflammation.
Neumann A, Küçükali F, Bos I, Vos SJB, Engelborghs S, De Pooter T, Joris G, De Rijk P, De Roeck E, Tsolaki M, Verhey F, Martinez-Lage P, Tainta M, Frisoni G, Blin O, Richardson J, Bordet R, Scheltens P, Popp J, Peyratout G, Johannsen P, Frölich L, Vandenberghe R, Freund-Levi Y, Streffer J, Lovestone S, Legido-Quigley C, Ten Kate M, Barkhof F, Strazisar M, Zetterberg H, Bertram L, Visser PJ, van Broeckhoven C, Sleegers K; EMIF-AD study group.
Neumann A, et al.
Mol Psychiatry. 2022 Apr;27(4):1990-1999. doi: 10.1038/s41380-022-01437-6. Epub 2022 Feb 16.
Mol Psychiatry. 2022.
PMID: 35173266
Free PMC article.
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