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Complement receptor 1 gene (CR1) intragenic duplication and risk of Alzheimer’s disease
Single nucleotide variants (SNVs) within and surrounding the complement receptor 1 (CR1) gene show some of the strongest genome-wide association signals with late-onset Alzheimer’s disease. Some studies have suggested that this association signal is due to a duplication allele (CR1-B) of a low copy...
Tallennettuna:
| Julkaisussa: | Hum Genet |
|---|---|
| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Springer Berlin Heidelberg
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5937907/ https://ncbi.nlm.nih.gov/pubmed/29675612 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-018-1883-2 |
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