第一作者:
Mary Pat,Reeve
第一单位:
Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.;Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.;Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA.
作者:
医学主题词
人类(Humans);黄斑变性(Macular Degeneration);老年人(Aged);男(雄)性(Male);女(雌)性(Female);补体因子H(Complement Factor H);疾病遗传易感性(Genetic Predisposition to Disease);单倍型(Haplotypes);老年人, 80以上(Aged, 80 and over);补体激活(Complement Activation);中年人(Middle Aged);多态性, 单核苷酸(Polymorphism, Single Nucleotide);补体C3b灭活蛋白质类(Complement C3b Inactivator Proteins);移码突变(Frameshift Mutation);病例对照研究(Case-Control Studies);视网膜(Retina);突变, 误义(Mutation, Missense);补体系统蛋白质类(Complement System Proteins)
DOI
10.1038/s41467-025-61193-3
PMID
40593839
发布时间
2025-07-08
基金项目
R01 MH115957/MH/NIMH NIH HHS/United States
R56 MH115957/MH/NIMH NIH HHS/United States
U24 HG011450/HG/NHGRI NIH HHS/United States
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