Association between a 45-bp 3'untranslated insertion/deletion polymorphism in exon 8 of UCP2 gene and neural tube defects in a high-risk area of China.
作者:
主题词
成年人(Adult);碱基序列(Base Sequence);中国(China);教育程度(Educational Status);外显子(Exons);女(雌)性(Female);叶酸(Folic Acid);基因频率(Gene Frequency);遗传关联研究(Genetic Association Studies);人类(Humans);INDEL突变(INDEL Mutation);婴儿, 新生(Infant, Newborn);离子通道(Ion Channels);线粒体蛋白质类(Mitochondrial Proteins);分子序列数据(Molecular Sequence Data);神经管缺损(Neural Tube Defects);多态现象, 遗传(Polymorphism, Genetic);妊娠(Pregnancy);危险(Risk);非翻译区(Untranslated Regions);青年人(Young Adult)
DOI
10.1177/1933719110393026
PMID
21266666
发布时间
2016-11-25
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