Examinations of methylenetetrahydrofolate reductase C677T and A1298C mutations--and in utero viability.
作者信息
Volcik K A, Blanton S H, Northrup H
出版信息
Am J Hum Genet. 2001 Nov;69(5):1150-3. doi: 10.1086/324066.
Abstract
摘要
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本文引用的文献
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Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations.新生儿和胎儿亚甲基四氢叶酸还原酶基因多态性：C677T和A1298C突变检测
Am J Hum Genet. 2000 Oct;67(4):986-90. doi: 10.1086/303082. Epub 2000 Aug 24.
3
A common mutation A1298C in human methylenetetrahydrofolate reductase gene: association with plasma total homocysteine and folate concentrations.人类亚甲基四氢叶酸还原酶基因常见突变A1298C：与血浆总同型半胱氨酸及叶酸浓度的关联
J Nutr. 1999 Sep;129(9):1656-61. doi: 10.1093/jn/129.9.1656.
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A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity.亚甲基四氢叶酸还原酶（MTHFR）中的第二种基因多态性与酶活性降低有关。
Mol Genet Metab. 1998 Jul;64(3):169-72. doi: 10.1006/mgme.1998.2714.
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