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

4 January 2017

title

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

1 reference

Glutamate ionotropic receptor NMDA type subunit 2D

4 January 2017

main subject

1 reference

ionotropic glutamate receptor activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Hakon Hakonarson

22

0 references

Xilma R Ortiz-Gonzalez

object named as

Xilma R. Ortiz-Gonzalez

3

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author name string

Dong Li

1

1 reference

4 January 2017

Hongjie Yuan

2

1 reference

4 January 2017

Eric D. Marsh

4

1 reference

4 January 2017

Lifeng Tian

5

1 reference

4 January 2017

Elizabeth M. McCormick

6

1 reference

4 January 2017

Gabrielle J. Kosobucki

7

1 reference

4 January 2017

Wenjuan Chen

8

1 reference

4 January 2017

Anthony J. Schulien

9

1 reference

4 January 2017

Rosetta Chiavacci

10

1 reference

4 January 2017

Anel Tankovic

11

1 reference

4 January 2017

Claudia Naase

12

1 reference

4 January 2017

Frieder Brueckner

13

1 reference

4 January 2017

Celina von Stülpnagel-Steinbeis

14

1 reference

4 January 2017

Chun Hu

15

1 reference

4 January 2017

Hirofumi Kusumoto

16

1 reference

4 January 2017

Ulrike B. S. Hedrich

17

1 reference

4 January 2017

Gina Elsen

18

1 reference

4 January 2017

Konstanze Hörtnagel

19

1 reference

4 January 2017

Elias Aizenman

20

1 reference

4 January 2017

Johannes R. Lemke

21

1 reference

4 January 2017

Stephen F. Traynelis

23

1 reference

4 January 2017

Marni J. Falk

24

1 reference

4 January 2017

language of work or name

English

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publication date

6 October 2016

1 reference

American Journal of Human Genetics

4 January 2017

published in

1 reference

4 January 2017

volume

99

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4 January 2017

issue

4

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4 January 2017

page(s)

802–816

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Memory and the NMDA receptors

4 January 2017

cites work

1 reference

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inferred from PubMed ID database lookup

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based on heuristic

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1 reference

https://pubmed.ncbi.nlm.nih.gov/27616483

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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1 reference

https://pubmed.ncbi.nlm.nih.gov/27616483

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.AJHG.2016.07.013

0 references

PMC publication ID

5065652

0 references

1 reference