A patient with classic Rett syndrome with a novel mutation in MECP2 exon 1

被引：19

作者：

Chunshu, Y.

Endoh, K.

Soutome, M.

Kawamura, R.

Kubota, T.

机构：

[1] Univ Yamanashi, Dept Epigenet Med, Yamanashi, Japan

[2] Hiroshima City Ctr Handicapped Children, Hiroshima, Hiroshima, Japan

来源：

CLINICAL GENETICS | 2006年 / 70卷 / 06期

关键词：

D O I：

10.1111/j.1399-0004.2006.00712.x

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：530 / 531

页数：2

共 11 条

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