About this item:

301 Views | 445 Downloads

Author Notes:

Correspondence: Dr. Hongjie Yuan, E-mail: hyuan@emory.edu

The author(s) have declared that no competing interests exist.



  • Epilepsy
  • GluN1
  • NDMA receptors
  • Neurology
  • Seizure disorders

GRIN1 Mutations in Early-Onset Epileptic Encephalopathy.


Journal Title:

Pediatric Neurology Briefs


Volume 29, Number 6


, Pages 44-44

Type of Work:

Article | Final Publisher PDF


Investigators from Yokohama City University and other medical centers in Israel and Japan reported mutations on N-methyl-D-aspartate (NMDA) receptors subunit GRIN1 (GluN1) identified in patients with nonsyndromic intellectual disability and early-onset epileptic encephalopathy.

Copyright information:

© 2015 The Author(s)

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/).

Creative Commons License

Export to EndNote