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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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| Publicado no: | JAMA Netw Open |
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Medical Association
2019
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| Assuntos: | |
| Acesso em linha: | 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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