Differences in methylenetetrahydrofolate reductase genotype frequencies, between Whites and Blacks.
作者信息
Stevenson R E, Schwartz C E, Du Y Z, Adams M J
出版信息
Am J Hum Genet. 1997 Jan;60(1):229-30.
Abstract
摘要
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本文引用的文献
1
5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects.
Am J Med Genet. 1996 Jun 28;63(4):610-4. doi: 10.1002/(SICI)1096-8628(19960628)63:4<610::AID-AJMG15>3.0.CO;2-L.
2
Nutritional ecogenetics: homocysteine-related arteriosclerotic vascular disease, neural tube defects, and folic acid.
Am J Hum Genet. 1996 Jan;58(1):17-20.
3
Spina bifida, 677T-->C mutation, and role of folate.
Lancet. 1995;346(8991-8992):1703. doi: 10.1016/s0140-6736(95)92865-0.
4
A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects.
QJM. 1995 Nov;88(11):763-6.
5
A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase.
Nat Genet. 1995 May;10(1):111-3. doi: 10.1038/ng0595-111.
6
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida.
Lancet. 1995 Oct 21;346(8982):1070-1. doi: 10.1016/s0140-6736(95)91743-8.
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