High prevalence of SLC6A8 deficiency, a novel X-linked mental retardation syndrome.

被引：0

作者：

Rosenberg, EH

Kleefstra, T

Wood, T

Almeida, L

Yntema, HG

Clark, AJ

Degrauw, RS

Bahi, N

Stevenson, RE

Moraine, C

Ropers, HH

Fryns, JP

DeGrauw, TJ

Jakobs, C

Schwartz, CE

Salomons, GS

机构：

[1] Vrije Univ Amsterdam, Med Ctr, Metab Unit, Dept Clin Chem, NL-1081 HV Amsterdam, Netherlands

[2] Univ Nijmegen, Med Ctr, Dept Human Genet, Nijmegen, Netherlands

[3] Greenwood Genet Ctr, JC Self Res Inst, Greenwood, SC 29646 USA

[4] CHU Cochin, INSERM, CNRS, Inst Cochin Genet Mol, Paris, France

[5] CHU Bretonneau, INSERM, U316, F-37044 Tours, France

[6] Max Planck Inst Mol Genet, Berlin, Germany

[7] Clin Genet Unit, Louvain, Belgium

[8] Cincinnati Childrens Hosp, Med Ctr, Cincinnati, OH USA

来源：

关键词：

D O I：

暂无

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：204 / 204

页数：1