MeCP2 mutations and gastrointestinal phenotype in Rett Syndrome

被引：0
|
作者：
Bibat, G
Cuffari, C
Naidu, S
机构：
[1] Kennedy Krieger Inst, Neurogenet Unit, Baltimore, MD USA
[2] Johns Hopkins Hosp, Div Pediat Gastroenterol, Baltimore, MD 21287 USA
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2003年 / 73卷 / 05期
关键词：
D O I：
暂无
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
598
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收藏
页码：272 / 272
页数：1
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