换一批High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts.
第一作者：
Megha N,Murthy
第一单位：
a Genetics and Genomics Lab, Department of Genetics and Genomics , University of Mysore , Mysore , India.
作者：
医学主题词
算法(Algorithms);队列研究(Cohort Studies);DNA拷贝数变异(DNA Copy Number Variations);数据库, 遗传学(Databases, Genetic);女(雌)性(Female);基因表达谱(Gene Expression Profiling);基因调控网络(Gene Regulatory Networks);疾病遗传易感性(Genetic Predisposition to Disease);全基因组关联研究(Genome-Wide Association Study);基因型(Genotype);人类(Humans);男(雄)性(Male);寡核苷酸序列分析(Oligonucleotide Array Sequence Analysis);帕金森病(Parkinson Disease);表型(Phenotype);质子转运ATP酶类(Proton-Translocating ATPases);泛素蛋白连接酶类(Ubiquitin-Protein Ligases)
DOI
10.1080/01616412.2016.1204105
PMID
27399248
发布时间
2022-03-17
- 浏览58
Neurological research
775-85页
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文
