Refining the phenotype of common mutations in Rett syndrome

被引：65

作者：

Colvin, L

Leonard, H

de Klerk, N

Davis, M

Weaving, L

Williamson, S

Christodoulou, J

机构：

[1] Univ Western Australia, Ctr Child Hlth Res, Telethon Inst Child Hlth Res, Perth, WA 6009, Australia

[2] Univ Western Australia, Ctr Neuromuscular & Neurol Disorders, Nedlands, WA 6009, Australia

[3] Univ Sydney, Discipline Paediat & Child Hlth, Sydney, NSW 2006, Australia

[4] Childrens Hosp, Western Sydney Genet Program, Westmead, NSW, Australia

来源：

JOURNAL OF MEDICAL GENETICS | 2004年 / 41卷 / 01期

关键词：

D O I：

10.1136/jmg.2003.011130

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：25 / 30

页数：6

共 43 条

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