Association of Rare Coding Mutations With Alzheimer Disease and Other Dementias Among Adults of European Ancestry

IMPORTANCE: Some of the unexplained heritability of Alzheimer disease (AD) may be due to rare variants whose effects are not captured in genome-wide association studies because very large samples are needed to observe statistically significant associations. OBJECTIVE: To identify genetic variants as...

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Opis bibliograficzny
Wydane w:JAMA Netw Open
Główni autorzy: Patel, Devanshi, Mez, Jesse, Vardarajan, Badri N., Staley, Lyndsay, Chung, Jaeyoon, Zhang, Xiaoling, Farrell, John J., Rynkiewicz, Michael J., Cannon-Albright, Lisa A., Teerlink, Craig C., Stevens, Jeffery, Corcoran, Christopher, Gonzalez Murcia, Josue D., Lopez, Oscar L., Mayeux, Richard, Haines, Jonathan L., Pericak-Vance, Margaret A., Schellenberg, Gerard, Kauwe, John S. K., Lunetta, Kathryn L., Farrer, Lindsay A.
Format: Artigo
Język:Inglês
Wydane: American Medical Association 2019
Hasła przedmiotowe:
Original Investigation
Dostęp online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6450321/
https://ncbi.nlm.nih.gov/pubmed/30924900
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamanetworkopen.2019.1350
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