MUTATIONS IN GRIN2B IN WEST SYNDROME AND INTELLECTUAL DISABILITY WITH CHILDHOOD-ONSET FOCAL EPILEPSY

被引：0

作者：

Lemke, J. R. ^{[1
,2
]}

Hendrickx, R. ^{[3
]}

Geider, K. ^{[4
]}

Bodo, L. ^{[4
]}

Schwake, M. ^{[5
]}

Harvey, R. J. ^{[6
]}

James, V. M. ^{[6
]}

Pepler, A. ^{[6
,7
]}

Steiner, I ^{[7
]}

Hoertnagel, K. ^{[7
]}

Neidhardt, J. ^{[8
]}

Ruf, S. ^{[9
]}

Wolff, M. ^{[9
]}

Bartholdi, D. ^{[10
]}

Caraballo, R. ^{[11
]}

Platzer, K. ^{[12
]}

Suls, A. ^{[3
]}

De Jonghe, P. ^{[3
]}

Biskup, S. ^{[7
,10
]}

Weckhuysen, S. ^{[3
]}

机构：

[1] Univ Leipzig, D-04109 Leipzig, Germany

[2] Univ Bern, Bern, Switzerland

[3] Univ Antwerp, B-2020 Antwerp, Belgium

[4] Tech Univ Darmstadt, Darmstadt, Germany

[5] Univ Bielefeld, D-33615 Bielefeld, Germany

[6] UCL, Sch Pharm, London, England

[7] CeGaT GmbH Ctr Genom & Transcript, Tubingen, Germany

[8] Univ Zurich, Zurich, Switzerland

[9] Univ Tubingen, Tubingen, Germany

[10] Klinikum Stuttgart, Inst Clin Genet, Stuttgart, Germany

[11] Juan P Garrahan Pediat Hosp, Buenos Aires, DF, Argentina

[12] Med Univ Lubeck, D-23538 Lubeck, Germany

来源：

EPILEPSIA | 2014年 / 55卷

关键词：

D O I：

暂无

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

020

引用

页码：11 / 11

页数：1

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