Mutations in SWI/SNF chromatin remodeling complex gene ARID1B cause Coffin-Siris syndrome

被引：0

作者：

Gijs W E Santen

Emmelien Aten

Yu Sun

Rowida Almomani

Christian Gilissen

Maartje Nielsen

Sarina G Kant

Irina N Snoeck

Els A J Peeters

Yvonne Hilhorst-Hofstee

Marja W Wessels

Nicolette S den Hollander

Claudia A L Ruivenkamp

Gert-Jan B van Ommen

Martijn H Breuning

Johan T den Dunnen

Arie van Haeringen

Marjolein Kriek

机构：

[1] Center for Human and Clinical Genetics,Department of Human Genetics

[2] Leiden University Medical Center,Department of Child Neurology

[3] Nijmegen Centre for Molecular Life Sciences and Institute for Genetic and Metabolic Disorders,Department of Clinical Genetics

[4] Radboud University Nijmegen Medical Centre,Department of Clinical Genetics

[5] Juliana Children's Hospital–Haga Teaching Hospital,undefined

[6] Erasmus Medical Center,undefined

[7] Leiden Genome Technology Center,undefined

[8] Leiden University Medical Center,undefined

[9] Juliana Children's Hospital–Haga Teaching Hospital,undefined

来源：

Nature Genetics | 2012年 / 44卷

关键词：

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Gijs Santen and colleagues report mutations in the SWI/SNF subunit gene ARID1B in Coffin-Siris syndrome.

引用

页码：379 / 380

页数：1

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