Comparative frequency of fragile-X (FMR1) and creatine transporter (SLC6A8) mutations in X-linked mental retardation

被引：7

作者：

Mandel, JL ^{[1
]}

机构：

[1] Univ Strasbourg 1, Coll France, IGBMC, CNRS,INSERM, F-67404 Illkirch Graffenstaden, CU Strasbourg, France

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 2004年 / 75卷 / 04期

关键词：

D O I：

10.1086/424821

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：730 / 731

页数：2

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