GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers (Q28119074)

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GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers
scientific journal article

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    GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers (English)
    1 reference
    0 references
    Dong Li
    1 reference
    Hongjie Yuan
    1 reference
    Eric D. Marsh
    1 reference
    Lifeng Tian
    1 reference
    Elizabeth M. McCormick
    1 reference
    Gabrielle J. Kosobucki
    1 reference
    Wenjuan Chen
    1 reference
    Anthony J. Schulien
    1 reference
    Rosetta Chiavacci
    1 reference
    Anel Tankovic
    1 reference
    Claudia Naase
    1 reference
    Frieder Brueckner
    1 reference
    Celina von Stülpnagel-Steinbeis
    1 reference
    Chun Hu
    1 reference
    Hirofumi Kusumoto
    1 reference
    Ulrike B. S. Hedrich
    1 reference
    Gina Elsen
    1 reference
    Konstanze Hörtnagel
    1 reference
    Elias Aizenman
    1 reference
    Johannes R. Lemke
    1 reference
    Stephen F. Traynelis
    1 reference
    Marni J. Falk
    1 reference
    6 October 2016
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    99
    1 reference
    802–816
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    4
    1 reference

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