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...

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Detalles Bibliográficos
Autores principales: Kucukkilic, Ezgi, Brookes, Keeley, Barber, Imelda, Guetta-Baranes, Tamar, Morgan, Kevin, Hollox, Edward J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937907/
https://www.ncbi.nlm.nih.gov/pubmed/29675612
http://dx.doi.org/10.1007/s00439-018-1883-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5937907/
https://www.ncbi.nlm.nih.gov/pubmed/29675612
http://dx.doi.org/10.1007/s00439-018-1883-2

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