Rett syndrome is caused by mutations in the X-linked MECP2 gene encoding methyl-CpG-binding protein

被引：0
|
作者：
Zoghbi, HY
Amir, RE
Wan, M
Lee, SS
Van den Veyver, IB
Tran, CQ
Malicki, D
Schanen, NC
Francke, U
机构：
[1] Howard Hughes Med Inst, Houston, TX 77030 USA
[2] Baylor Coll Med, Houston, TX 77030 USA
[3] Stanford Univ, Stanford, CA 94305 USA
[4] Univ Calif Los Angeles, Los Angeles, CA USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2000年 / 66卷 / 05期
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D O I：
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中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
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页码：1723 / 1723
页数：1
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