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GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers
2016
179 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
19.24
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers | Researchclopedia
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University of Pittsburgh
Wenjuan Chen
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Emory University
Anthony J. Schulien
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University of Pittsburgh
Rosetta Chiavacci
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Children's Hospital of Philadelphia
Anel Tankovic
·
Emory University
Claudia Naase
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Bayreuth Medical Center
F Brueckner
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Hamburg Institute for Social Research
Celina von Stülpnagel-Steinbeis
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Paracelsus Medical University
Chun Hu
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Emory University
Hirofumi Kusumoto
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Emory University
Ulrike B. S. Hedrich
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Hertie Institute for Clinical Brain Research
Gina E. Elsen
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Hertie Institute for Clinical Brain Research
Konstanze Hörtnagel
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CeGaT (Germany)
Elias Aizenman
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University of Pittsburgh
Johannes R. Lemke
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University Hospital Leipzig
Håkon Håkonarson
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Children's Hospital of Philadelphia
Stephen F. Traynelis
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Emory University
Marni J. Falk
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Children's Hospital of Philadelphia