Human genetics: Methylation moves into medicine

被引：16
|
作者：
Hendrich, B [1 ]
机构：
[1] Univ Edinburgh, Inst Cell & Mol Biol, Edinburgh EH9 3JR, Midlothian, Scotland
来源：
CURRENT BIOLOGY | 2000年 / 10卷 / 02期
关键词：
D O I：
10.1016/S0960-9822(00)00286-4
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
Two human genetic diseases have recently been shown to be due to mutations in genes encoding proteins involved in DNA methylation. The phenotypes of these two diseases are surprisingly distinct from each other and provide insights into the functions of DNA methylation in mammals.
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收藏
页码：R60 / R63
页数：4
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