Rett syndrome: analysis of MECP2 mutations in Brazilian patients.

被引：0
|
作者：
Lima, FT
Vasques, LR
Garcia, SMN
Kok, F
Otto, PG
Pereira, LV
机构：
[1] EPM UNIFESP, Ctr Genet Med, Sao Paulo, Brazil
[2] Univ Sao Paulo, Dept Biol IB, Sao Paulo, Brazil
[3] Univ Sao Paulo, Dept Neurol FM, Sao Paulo, Brazil
来源：
AMERICAN JOURNAL OF HUMAN GENETICS | 2000年 / 67卷 / 04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：
2260
引用
收藏
页码：402 / 402
页数：1
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