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Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes
2010
506 citations
Journal Article
Field-Weighted Citation Impact:
9.87
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes | Researchclopedia
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Hôpital de la Timone
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Universität Hamburg
Angela Fritsch
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Universität Hamburg
Friederike K Pientka
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Universität Hamburg
Yorck Hellenbroich
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University of Lübeck
Vera M. Kalscheuer
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Max Planck Society
Jürgen Kohlhase
Ute Moog
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Heidelberg University
Gudrun Rappold
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Heidelberg University
Anita Rauch
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Friedrich-Alexander-Universität Erlangen-Nürnberg
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Max Planck Institute for Molecular Genetics
Sarah von Spiczak
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Kiel University
Holger Tönnies
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Clinical Research Center Kiel
Nathalie Villeneuve
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Henri Gastaut Hospital
Laurent Villard
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Institut de Neurobiologie de la Méditerranée
Bernhard Zabel
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University Medical Center Freiburg
Martin Zenker
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University of Lübeck
Bodo Laube
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Technical University of Darmstadt
André Reis
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Friedrich-Alexander-Universität Erlangen-Nürnberg
Dagmar Wieczorek
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Essen University Hospital
Lionel Van Maldergem
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Centre Hospitalier Universitaire de Liège
Kerstin Kutsche
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University Medical Center Hamburg-Eppendorf