Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome

被引：47
|
作者：
Obata, K
Matsuishi, T
Yamashita, Y
Fukuda, T
Kuwajima, K
Horiuchi, I
Nagamitsu, S
Iwanaga, R
Kimura, A
Omori, I
Endo, S
Mori, K
Kondo, I
机构：
[1] Kurume Univ, Sch Med, Dept Paediat & Child Hlth, Kurume, Fukuoka 8300011, Japan
[2] Ibaraki Handicapped Childrens Ctr, Dept Paediat, Mito, Ibaraki 3100008, Japan
[3] Asahigawa Jidoin Childrens Hosp, Okayama 7038555, Japan
[4] Okayama Univ, Sch Med, Dept Child Neurol, Okayama 7008558, Japan
[5] Natl Kagawa Childrens Hosp, Dept Paediat, Kagawa 7658501, Japan
[6] Univ Tokushima, Sch Med, Dept Paediat, Tokushima 7708503, Japan
来源：
JOURNAL OF MEDICAL GENETICS | 2000年 / 37卷 / 08期
关键词：
D O I：
10.1136/jmg.37.8.608
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：608 / 610
页数：3
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