Comprehensive mutation analysis of the MECP2 gene and the analysis of 54 Rett syndrome suspected patients

被引：0
|
作者：
Vos, YJ
Mol, GJJ
Begeer, JH
Verlind, E
van den Akker, PC
Buys, CHCM
Hordijk, R
Hofstra, RMW
机构：
[1] Univ Groningen Hosp, Dept Clin Genet, Groningen, Netherlands
[2] Univ Groningen Hosp, Dept Neurol, Groningen, Netherlands
[3] Univ Groningen, Dept Med Genet, NL-9700 AB Groningen, Netherlands
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2002年 / 10卷
关键词：
D O I：
暂无
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：
引用
收藏
页码：230 / 230
页数：1
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