早发性阿尔茨海默病
疾病
生物
遗传学
全基因组关联研究
基因组学
计算生物学
阿尔茨海默病
医学
基因组
基因
单核苷酸多态性
病理
基因型
作者
Nicholas R. Ray,Temitope Ayodele,Melissa Jean‐Francois,Penelope Baez,María Victoria Fernández,Joseph Bradley,Paul K. Crane,Clifton L. Dalgard,Amanda B Kuzma,Heather Nicaretta,Rebecca Sims,Julie Williams,Michael L. Cuccaro,Margaret A. Pericak‐Vance,Richard Mayeux,Weixin Wang,Gerard D. Schellenberg,Carlos Cruchaga,Gary W. Beecham,Christiane Reitz
摘要
Sequencing efforts to identify genetic variants and pathways underlying Alzheimer's disease (AD) have largely focused on late-onset AD although early-onset AD (EOAD), accounting for ∼10% of cases, is largely unexplained by known mutations, resulting in a lack of understanding of its molecular etiology.
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