德鲁森
黄斑变性
遗传学
生物
基因型
单核苷酸多态性
基因
系数H
多态性(计算机科学)
等位基因
发起人
医学
补体系统
眼科
基因表达
抗体
作者
Andrew T. DeWan,Mugen Liu,Stephen E. Hartman,Samuel Shao-Min Zhang,David T.L. Liu,Connie Zhao,Pancy O. S. Tam,Wai Man Chan,Dennis S.C. Lam,M Snyder,Colin J. Barnstable,Chi Pui Pang,Josephine Hoh
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2006-10-20
卷期号:314 (5801): 989-992
被引量:867
标识
DOI:10.1126/science.1133807
摘要
Age-related macular degeneration (AMD), the most common cause of irreversible vision loss in individuals aged older than 50 years, is classified as either wet (neovascular) or dry (nonneovascular). Inherited variation in the complement factor H gene is a major risk factor for drusen in dry AMD. Here we report that a single-nucleotide polymorphism in the promoter region of HTRA1 , a serine protease gene on chromosome 10q26, is a major genetic risk factor for wet AMD. A whole-genome association mapping strategy was applied to a Chinese population, yielding a P value of <10 –11 . Individuals with the risk-associated genotype were estimated to have a likelihood of developing wet AMD 10 times that of individuals with the wild-type genotype.
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