TYROBP genetic variants in early-onset Alzheimer’s disease

We aimed to identify new candidate genes potentially involved in early onset Alzheimer’s disease (EOAD). Exome sequencing was conducted on 45 EOAD patients with either a family history of Alzheimer’s disease (AD, <65 years) or an extremely early age at onset (≤55 years) followed by multiple varia...

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Detalhes bibliográficos
Publicado no:Neurobiol Aging
Main Authors: Pottier, Cyril, Ravenscroft, Thomas A., Brown, Patricia H., Finch, NiCole A., Baker, Matt, Parsons, Meeia, Asmann, Yan W., Ren, Yingxue, Christopher, Elizabeth, Levitch, Denise, van Blitterswijk, Marka, Cruchaga, Carlos, Campion, Dominique, Nicolas, Gaël, Richard, Anne-Claire, Guerreiro, Rita, Bras, Jose T., Zuchner, Stephan, Gonzalez, Michael A., Bu, Guojun, Younkin, Steven, Knopman, David S., Josephs, Keith A., Parisi, Joseph E., Petersen, Ronald C., Ertekin-Taner, Nilüfer, Graff-Radford, Neill R., Boeve, Bradley F., Dickson, Dennis W., Rademakers, Rosa
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5159294/
https://ncbi.nlm.nih.gov/pubmed/27658901
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neurobiolaging.2016.07.028
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