Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.
第一作者:
Lisa,Skipper
第一单位:
Population Genetics, Genome Institute of Singapore, Singapore.
作者:
主题词
成年人(Adult);老年人(Aged);老年人, 80以上(Aged, 80 and over);女(雌)性(Female);基因频率(Gene Frequency);疾病遗传易感性(Genetic Predisposition to Disease);单倍型(Haplotypes);人类(Humans);连锁不平衡(Linkage Disequilibrium);男(雄)性(Male);中年人(Middle Aged);帕金森病(Parkinson Disease);多态性, 单核苷酸(Polymorphism, Single Nucleotide);危险因素(Risk Factors)
DOI
10.1093/hmg/ddi376
PMID
16269443
发布时间
2022-12-07
- 浏览20

Human molecular genetics
3549-56页
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