A new regulatory pathway for fragile X syndrome?

被引：0
|
作者：
R. Scott Hansen
Charles D. Laird
机构：
[1] Division of Medical Genetics University of Washington,
[2] Department of Zoology University of Washington,undefined
来源：
Nature Medicine | 2002年 / 8卷
关键词：
D O I：
暂无
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学科分类号：
摘要：
One out of every 4,500 males suffers cognitive impairment due to alterations in the fragile X gene. The gene has a complicated biology, and it may have just gotten a bit more complex. The fragile X gene product in flies could play a role in regulation by small RNA molecules.
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页码：1204 / 1205
页数：1
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