换一批
换一批Association of COMT, MTHFR, and SLC19A1(RFC-1) polymorphisms with homocysteine blood levels and cognitive impairment in Parkinson's disease.
作者：
主题词
儿茶酚O-甲基转移酶(Catechol O-Methyltransferase);认知障碍(Cognition Disorders);女(雌)性(Female);叶酸(Folic Acid);遗传关联研究(Genetic Association Studies);疾病遗传易感性(Genetic Predisposition to Disease);高半胱氨酸(Homocysteine);人类(Humans);男(雄)性(Male);亚甲基四氢叶酸还原酶(NADPH)(Methylenetetrahydrofolate Reductase (NADPH2));帕金森病(Parkinson Disease);多态现象, 遗传(Polymorphism, Genetic);还原叶酸载体蛋白(Reduced Folate Carrier Protein);维生素B12(Vitamin B 12)
DOI
10.1097/FPC.0b013e32835693f7
PMID
22890010
发布时间
2013-11-21
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