换一批Direct or indirect association in a complex disease: the role of SLC22A4 and SLC22A5 functional variants in Crohn disease.
第一作者：
Sheila A,Fisher
第一单位：
Department of Medical and Molecular Genetics, King's College London School of Medicine, Guy's Hospital, London, United Kingdom.
作者：
医学主题词
病例对照研究(Case-Control Studies);队列研究(Cohort Studies);Crohn病(Crohn Disease);DNA突变分析(DNA Mutational Analysis);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);多基因族(Multigene Family);有机阳离子转运蛋白质类(Organic Cation Transport Proteins);多态性, 单核苷酸(Polymorphism, Single Nucleotide);协同转运子(Symporters)
DOI
10.1002/humu.20358
PMID
16835882
发布时间
2020-12-09
基金项目
Wellcome Trust/United Kingdom
- 浏览37
Human mutation
778-85页
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