GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers-Reference-Cited by-同舟云学术

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

Published:2016-10 Issue:4 Volume:99 Page:802-816
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Li Dong,Yuan Hongjie,Ortiz-Gonzalez Xilma R.,Marsh Eric D.,Tian Lifeng,McCormick Elizabeth M.,Kosobucki Gabrielle J.,Chen Wenjuan,Schulien Anthony J.,Chiavacci Rosetta,Tankovic Anel,Naase Claudia,Brueckner Frieder,von Stülpnagel-Steinbeis Celina,Hu Chun,Kusumoto Hirofumi,Hedrich Ulrike B.S.,Elsen Gina,Hörtnagel Konstanze,Aizenman Elias,Lemke Johannes R.,Hakonarson Hakon,Traynelis Stephen F.,Falk Marni J.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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